Tekna · Monoplace
Tekna Hybrid 4000 Monoplace
The Tekna Hybrid 4000 Monoplace is a monoplace hyperbaric chamber operating at up to 3 ATA for 1 patient.
Operating pressure3 ATACapacity1 patientChamber typeMonoplace
Overview
The Tekna Hybrid 4000 Monoplace is a monoplace hyperbaric chamber operating at up to 3 ATA for 1 patient. Single-occupant rigid chambers built for clinical-grade pressure in one treatment room.
Highlights
- Wider 40 in bore for roomier interior vs. the 3200
- Integrated patient stretcher, 750 lb capacity (no separate gurney)
- 100% oxygen, up to ~29.4 psi
- Bio-compatible interior finishes
How we verify
Manufacturer-stated. Specifications for this model come from the manufacturer's own documentation and could not be confirmed in an independent register. We list them as stated and flag what is missing.
FDA 510(k) clearance is claimed on the product page but could not be confirmed: among the FDA CBF register entries only the Hybrid 3200 (K002795) and Model 5000 (K002794) appear. Clearance is likely being asserted by reference to those older Hypertec filings; treat the 4000-specific FDA claim as unverified.
Sources
Specifications
| Manufacturer | Tekna |
|---|---|
| Chamber type | Monoplace |
| Operating pressure | 3.0 |
| Capacity | 1 patient |
| Inner diameter | 40 in (101.6 cm) |
| Dimensions | Not published |
| Weight | Not published |
| Certifications | Website advertises 'FDA 510(k) Cleared' (Class B monoplace) but NO Hybrid 4000 entry exists in the FDA hyperbaric-chamber register (product code CBF); ASME / National Board / PVHO-1 / NFPA-99 (manufacturer-stated) |
| Price | Price on request |
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Tekna Model 5000
3–6 ATAConfigurable ~4 to 14+ occupants depending on diameter and lock count
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