K852127 is an FDA 510(k) clearance for the AMSCO URO-ENDO MOBILE TABLE. This device is classified as a Table, Cystometric, Non-electric And Accessories (Class I - General Controls, product code KQS).
Submitted by American Sterilizer Co. (Erie, US). The FDA issued a Cleared decision on August 8, 1985, 85 days after receiving the submission on May 15, 1985.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.4890.
| 510(k) Number | K852127 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 15, 1985 |
| Decision Date | August 08, 1985 |
| Days to Decision | 85 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | — |
| Product Code | KQS — Table, Cystometric, Non-electric And Accessories |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 876.4890 |