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

Adaptor, Bulbs, Miscellaneous, For Endoscope

21 CFR 876.1500 / Gastroenterology, Urology
FDA source (opens on fda.gov)

FFY is the FDA product code for Adaptor, Bulbs, Miscellaneous, For Endoscope, a class I device type, regulated under 21 CFR 876.1500. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FFY
Device name
Adaptor, Bulbs, Miscellaneous, For Endoscope
Regulation
21 CFR 876.1500
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
2
Ingested recalls
0

Clearances, product code FFY

By decision year
2 clearances under product code FFY with a decision year between 1990 and 1994, 1990 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FFY by decision year
YearClearances
19901
19941

Applicants with the most clearances

Product code FFY
Applicants holding the most 510(k) clearances under product code FFY
ApplicantClearances
Applied Urology, Inc.1
Columbia Medical & Surgical, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 87 companies shown, in name order