P AND T MEDIUM
FDA 510(k) clearance K904773 · decided 1990-12-04
Clearance details
- K-number
- K904773
- Device name
- P AND T MEDIUM
- Applicant
- Gibson Laboratories, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1990-10-22
- Decision date
- 1990-12-04
- Days to decision
- 43 days
- Clearance type
- Traditional
- Product code
- JTW
- Device class
- 1
- Regulation number
- 866.2900
- Medical specialty
- Microbiology
- Advisory committee
- Microbiology
- Location
- Lexington, KY, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.