510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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FFNClass I

Clamp, Non-Electrical

21 CFR 876.4730 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FFN is the FDA product code for Clamp, Non-Electrical, a class I device type, regulated under 21 CFR 876.4730. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FFN
Device name
Clamp, Non-Electrical
Regulation
21 CFR 876.4730
Device class
Class I
Review panel
Gastroenterology, Urology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
5
Ingested recalls
0

Clearances, product code FFN

By decision year
5 clearances under product code FFN with a decision year between 1977 and 1993, 1989 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code FFN by decision year
YearClearances
19771
19781
19892
19931

Applicants with the most clearances

Product code FFN
Applicants holding the most 510(k) clearances under product code FFN
ApplicantClearances
Zinnanti Surgical Instruments, Inc.2
Baxter Healthcare Corporation1
Fred Sammons, Inc.1
Quinton, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 56 companies shown, in name order