510(k) K771421
- Device
- Catheteo Clamp
- Applicant
- QUINTON, INC.
- 510(k) number
- K771421
- Product code
- FFN
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-10-25
- Date received
- 1977-08-01
- Regulation
- 876.4730
- Classification name
- Clamp, Non-Electrical
- Medical specialty
- Gastroenterology, Urology
- Review panel
- Gastroenterology, Urology
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3014334038
- 8010422
- 9680425
- 9611112
- 3005440795
- 3005809810
- 9710524
- 3007507973
- 3004215117
- 3011137372
- 8010370
- 1646747
- 8010374
- 3005067367
- 3006554912
- 1421879
- 3011270181
- 1056350
- 9612278
- 3004001706
- 1417592
- 1836161
- 9612086
- 3010041511
- 3035678069
- 8010099
- 1923569
- 3010687973
- 8040233
- 1424478
- 2916714
- 3035708926
- 3008770252
- 3003407244
- 1648701
- 9680518
- 9611283
- 3008711893
- 9612074
- 3007648354
- 3004608878
- 1421101
- 3010055973
- 8043467
- 8030607
- 2028411
- 1720747
- 2434839
- 9680519
- 9611503
- 3003418325
- 2531475
- 3005528784
- 9610612
- 8010665
- 3008808049
- 9680718
- 3015972835
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code FFN#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K932408 | AMBULATORY INFUSION PUMP SYSTEM AND SOLUTION SETS | Baxter Healthcare Corp | 1993-09-28 |
| K892542 | RECTAL SPECULA - CHELSEA-EATON, KELLY, MATHIEU | Zinnanti Surgical Instruments, Inc. | 1989-05-09 |
| K892550 | BEST COLON CLAMP | Zinnanti Surgical Instruments, Inc. | 1989-05-09 |
| K772405 | TUBING CLAMP | Fred Sammons, Inc. | 1978-01-26 |