FDA Product Code
FDA Product Code KQS — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Gastroenterology, Urology
- 21 CFR Citation
- 876.4890
510(k) Clearances — 8 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K955019 | UROTRACT I | Dornier Medtech America, Inc. | 1995-12-06 | Traditional | PDF ↗ |
| K872022 | UROVIEW | Oec-Diasonics, Inc. | 1987-07-16 | Traditional | PDF ↗ |
| K864846 | RADIOGRAPHIC - LEG SECTION | American Sterilizer Co. | 1986-12-24 | Traditional | PDF ↗ |
| K860040 | HYDRAJUST III UROLOGICAL TABLE | Mallinckrodt Group, Inc. | 1986-02-10 | Traditional | PDF ↗ |
| K852127 | AMSCO URO-ENDO MOBILE TABLE | American Sterilizer Co. | 1985-08-08 | Traditional | PDF ↗ |
| K801723 | UR 150-UR 150T | Siemens Corp. | 1980-08-13 | Traditional | PDF ↗ |
| K791699 | HYDRADJUST II UROLOGICAL TABLE | Sybron Corp. | 1979-10-22 | Traditional | PDF ↗ |
| K760522 | TABLE, UROSURGICAL | Mallinckrodt Group, Inc. | 1976-12-16 | Traditional | PDF ↗ |
Product code KQS · Class I · Gastroenterology, Urology. Data: openFDA.