K871234 is an FDA 510(k) clearance for the ANTIBODY ASSAY FOR DETECT. OF PARAINFLUENZA TYPE 1. This device is classified as a Antigens, Cf (including Cf Control), Parainfluenza Virus 1-4 (Class I - General Controls, product code GQS).
Submitted by Microscan Div. Baxter Healthcare Corp. (West Sacramento, US). The FDA issued a Cleared decision on June 26, 1987, 91 days after receiving the submission on March 27, 1987.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.3400.
| 510(k) Number | K871234 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 27, 1987 |
| Decision Date | June 26, 1987 |
| Days to Decision | 91 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | — |
| Product Code | GQS — Antigens, Cf (including Cf Control), Parainfluenza Virus 1-4 |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 866.3400 |