CIDEX FORMULA 7* LONG-LIFE ACTIVATED DIALDEHYDE
FDA 510(k) clearance K924334 · decided 1994-03-29
Clearance details
- K-number
- K924334
- Device name
- CIDEX FORMULA 7* LONG-LIFE ACTIVATED DIALDEHYDE
- Applicant
- Johnson & Johnson Medical, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1992-08-27
- Decision date
- 1994-03-29
- Days to decision
- 579 days
- Clearance type
- Traditional
- Product code
- MED
- Device class
- 2
- Regulation number
- 880.6885
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Arlington, TX, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Johnson & Johnson Medical
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.
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| BIO-SORB ABSORBABLE DUSTING POWDER (N6264/S003) | Johnson & Johnson Medical, Inc. | 1985-09-10 |