UR 150-UR 150T
FDA 510(k) clearance K801723 · decided 1980-08-13
Clearance details
- K-number
- K801723
- Device name
- UR 150-UR 150T
- Applicant
- Siemens Corp.
- Decision
- Substantially Equivalent
- Date received
- 1980-07-24
- Decision date
- 1980-08-13
- Days to decision
- 20 days
- Clearance type
- Traditional
- Product code
- KQS
- Device class
- 1
- Regulation number
- 876.4890
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| UROTRACT I (K955019) | Dornier Medtech America, Inc. | 1995-12-06 |
| UROVIEW (K872022) | Oec-Diasonics, Inc. | 1987-07-16 |
| RADIOGRAPHIC - LEG SECTION (K864846) | American Sterilizer Co. | 1986-12-24 |
| HYDRAJUST III UROLOGICAL TABLE (K860040) | Mallinckrodt Group, Inc. | 1986-02-10 |
| AMSCO URO-ENDO MOBILE TABLE (K852127) | American Sterilizer Co. | 1985-08-08 |
| HYDRADJUST II UROLOGICAL TABLE (K791699) | Sybron Corp. | 1979-10-22 |
| TABLE, UROSURGICAL (K760522) | Mallinckrodt Group, Inc. | 1976-12-16 |
Recalls involving this device
No recalls on record reference this clearance.