DISP. TEFLON CONNHCTOR
FDA 510(k) clearance K771429 · decided 1977-12-22
Clearance details
- K-number
- K771429
- Device name
- DISP. TEFLON CONNHCTOR
- Applicant
- Quinton, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1977-08-01
- Decision date
- 1977-12-22
- Days to decision
- 143 days
- Clearance type
- Traditional
- Product code
- FJQ
- Device class
- 1
- Regulation number
- 876.5540
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Quinton
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| SHUNT CONNECTORS (K893679) | Akcess Medical Products, Inc. | 1989-07-24 |
| PATIENT BY-PASS (K771422) | Quinton, Inc. | 1978-01-03 |
Recalls involving this device
No recalls on record reference this clearance.