RECTANGULAR MULTIPLACE HYPERBARIC CHAMBER
FDA 510(k) clearance K082455 · decided 2009-05-22
Clearance details
- K-number
- K082455
- Device name
- RECTANGULAR MULTIPLACE HYPERBARIC CHAMBER
- Applicant
- Gulf Coast Hyperbarics, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2008-08-26
- Decision date
- 2009-05-22
- Days to decision
- 269 days
- Clearance type
- Traditional
- Product code
- CBF
- Device class
- 2
- Regulation number
- 868.5470
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Lynn Haven, FL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Gulf Coast Hyperbarics
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.