DRYSLIDE CEFIN
FDA 510(k) clearance K930702 · decided 1993-12-22
Clearance details
- K-number
- K930702
- Device name
- DRYSLIDE CEFIN
- Applicant
- Difco Laboratories, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1993-02-10
- Decision date
- 1993-12-22
- Days to decision
- 315 days
- Clearance type
- Traditional
- Product code
- JTN
- Device class
- 2
- Regulation number
- 866.1620
- Medical specialty
- Microbiology
- Advisory committee
- Microbiology
- Location
- Detroit, MI, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Difco Laboratories
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.