K935987 is an FDA 510(k) clearance for the FLEXTRANS. This device is classified as a Culture Media, Non-propagating Transport (Class I - General Controls, product code JSM).
Submitted by Baxter Diagnostics, Inc. (Issaquash, US). The FDA issued a Cleared decision on August 15, 1994, 244 days after receiving the submission on December 14, 1993.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.2390.
| 510(k) Number | K935987 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 14, 1993 |
| Decision Date | August 15, 1994 |
| Days to Decision | 244 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | Summary PDF |
| Product Code | JSM — Culture Media, Non-propagating Transport |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 866.2390 |