510(k) K844121
- Device
- Clamp, Tubing, Line
- Applicant
- DYN-A-MED PRODUCTS
- 510(k) number
- K844121
- Product code
- FKK
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1984-12-17
- Date received
- 1984-10-23
- Regulation
- 876.4730
- Classification name
- Clamp, Line
- Medical specialty
- Gastroenterology, Urology
- Review panel
- Gastroenterology, Urology
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- RICHARD J VANNOTE
- Address
- 255 Bluff Ct. Barrington IL US 60010 60010
FDA Registration Numbers#
- 8020347
- 3032828299
- 9710524
- 3038195011
- 2314912
- 3010202439
- 1649518
- 2020550
- 3003504604
- 1836161
- 9611024
- 3014579161
- 8040233
- 2018692
- 3001644167
- 3010765841
- 8030607
- 9612168
- 3005907133
- 9611665
- 3016965929
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code FKK#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K854512 | TUBING CLAMP CAT#1000-A | Rao Medical Devices, Inc. | 1985-12-02 |
| K854517 | NEW TRAVENOL ROLLER CLAMP-SOLUTION ADMIN. SET | Travenol Laboratories, S.A. | 1985-12-02 |
| K831689 | EMPTY DIALYSATE CONTAINER | Delmed, Inc. | 1983-08-11 |
| K822551 | AMP CAPD UNISPIKE AMINISTRATION SET | American Medical Products, Inc. | 1982-10-13 |
| K802009 | FLOWCLAMP CAT.#1011 & 1012 | Pollak (Intl.), Ltd. | 1980-10-31 |