K872696 is an FDA 510(k) clearance for the PARAINFLUENZA-3-CF ANTIGEN AND CONTROL ANTIGEN. This device is classified as a Antisera, Cf, Parainfluenza Virus 1-4 (Class I - General Controls, product code GQT).
Submitted by Sita, Inc. (Allentown, US). The FDA issued a Cleared decision on September 18, 1987, 73 days after receiving the submission on July 7, 1987.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.3400.
| 510(k) Number | K872696 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 07, 1987 |
| Decision Date | September 18, 1987 |
| Days to Decision | 73 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | — |
| Product Code | GQT — Antisera, Cf, Parainfluenza Virus 1-4 |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 866.3400 |