510(k) K771419
- Device
- CANNULA CLAMP
- Applicant
- Quinton, Inc.
- 510(k) number
- K771419
- Product code
- FKC
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-08-26
- Date received
- 1977-08-01
- Regulation
- 876.5540
- Classification name
- Clamp, Cannula
- Medical specialty
- Gastroenterology, Urology
- Review panel
- Gastroenterology, Urology
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- N
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 8030607
- 3005273623
- 1646747
- 3006517555
- 3021091077
- 3011987967
- 3011137372
- 1833053
- 1018233
- 3004215117
- 3010041511
- 3003418325
- 8040278
- 1412854
- 3003431869
- 9611112
- 3032747418
- 3016965929
- 9617592
- 3008902714
- 1836161
- 3006260740
- 3008806809
- 3001644167
- 1835998
- 3006082230
Source Documents#
510(k) summary PDF not indicated by FDA