MUELLER HINTON BROTH
FDA 510(k) clearance K802957 · decided 1980-12-22
Clearance details
- K-number
- K802957
- Device name
- MUELLER HINTON BROTH
- Applicant
- Gibco Laboratories Life Technologies, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1980-11-17
- Decision date
- 1980-12-22
- Days to decision
- 35 days
- Clearance type
- Traditional
- Product code
- JTZ
- Device class
- 2
- Regulation number
- 866.1700
- Medical specialty
- Microbiology
- Advisory committee
- Microbiology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Gibco Laboratories Life Technologies
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
| Record | Firm | Date |
|---|---|---|
| 1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450 recall (Z-0585-2026) | Remel, Inc | 2025-11-21 |