510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K863752Substantially Equivalent

Valtrac (Bar) Remover Device

Davis & Geck, Inc., Danbury CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K863752 is the FDA 510(k) clearance record for VALTRAC (BAR) REMOVER DEVICE, a class I device, cleared for Davis & Geck, Inc. on under FDA product code EMF (Knife, Surgical). FDA records list 45 510(k) clearances for Davis & Geck, Inc., from to . As of , FDA records show no recalls naming K863752.

Clearance record

Decision date
Received
(29 days to decision)
Product code
EMF Knife, Surgical
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Davis & Geck, Inc. American Cynamid Company, Danbury CT
Third party review
No

Clearances, product code EMF

Trailing 12 months

FDA records hold no clearances under product code EMF in the trailing twelve months.

FDA records show no clearances under product code EMF in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EMF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260