HEMAWAY SEAT
FDA 510(k) clearance K072690 · decided 2007-12-07
Clearance details
- K-number
- K072690
- Device name
- HEMAWAY SEAT
- Applicant
- Hemaway, LLC
- Decision
- Substantially Equivalent
- Date received
- 2007-09-24
- Decision date
- 2007-12-07
- Days to decision
- 74 days
- Clearance type
- Traditional
- Product code
- LRL
- Device class
- U
- Medical specialty
- Unknown
- Advisory committee
- Unknown
- Location
- Wilmington, DE, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Hemaway
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.
| Record | Firm | Date |
|---|---|---|
| PERI-COMFORT(TM) SEATING CUSHION (K932396) | Chi'Am Intl. | 1993-09-30 |
| HEMOREST(TM) (K864470) | Health Aid Products | 1987-06-23 |
Recalls involving this device
No recalls on record reference this clearance.