K961730 is an FDA 510(k) clearance for the RAPID GRAM-POSITIVE ID SYSTEM. This device is classified as a Gram Positive Identification Panel (Class I - General Controls, product code LQL).
Submitted by Becton Dickinson Microbiology Systems (Cockeysville, US). The FDA issued a Cleared decision on February 4, 1997, 277 days after receiving the submission on May 3, 1996.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.2660.
| 510(k) Number | K961730 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 03, 1996 |
| Decision Date | February 04, 1997 |
| Days to Decision | 277 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | Statement |
| Product Code | LQL — Gram Positive Identification Panel |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 866.2660 |