Submission Details
| 510(k) Number | K961324 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | April 08, 1996 |
| Decision Date | July 02, 1996 |
| Days to Decision | 85 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | Statement |
K961324 is an FDA 510(k) clearance for the GLOBAL MEDICAL PRODUCTS SPINAL,CONICAL TIP (SPROTTLE STYLE), WHITACRE STYLE NEEDLES, a Needle, Spinal, Short Term (Class II — Special Controls, product code MIA), submitted by Global Medical Prods, Inc. (Oakville Ont.L6l 5k9, CA). The FDA issued a Cleared decision on July 2, 1996, 85 days after receiving the submission on April 8, 1996. This device falls under the Anesthesiology review panel. Regulated under 21 CFR 868.5150.
| 510(k) Number | K961324 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | April 08, 1996 |
| Decision Date | July 02, 1996 |
| Days to Decision | 85 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | Statement |
| Product Code | MIA — Needle, Spinal, Short Term |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 868.5150 |