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

Curette

21 CFR 878.4800 / General, Plastic Surgery
FDA source (opens on fda.gov)

HTF is the FDA product code for Curette, a class I device type, regulated under 21 CFR 878.4800. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
HTF
Device name
Curette
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
2

Clearances, product code HTF

By decision year
3 clearances under product code HTF with a decision year between 1984 and 1989, 1984 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HTF by decision year
YearClearances
19841
19871
19891

Applicants with the most clearances

Product code HTF
Applicants holding the most 510(k) clearances under product code HTF
ApplicantClearances
Buckman Co., Inc.1
Kinetic Medical Products1
Stainless Mfg., Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 299 companies shown, in name order