510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K891756Substantially Equivalent

Kinetic Model 500

Kinetic Biomedical Services, Inc., Erie PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K891756 is the FDA 510(k) clearance record for KINETIC MODEL 500, a class II device, cleared for Kinetic Biomedical Services, Inc. on under FDA product code FSY (Light, Surgical, Ceiling Mounted). FDA records list 5 510(k) clearances for Kinetic Biomedical Services, Inc., from to . As of , FDA records show no recalls naming K891756.

Clearance record

Decision date
Received
(27 days to decision)
Product code
FSY Light, Surgical, Ceiling Mounted
Regulation
21 CFR 878.4580
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Kinetic Biomedical Services, Inc. 4934 Peach St., Erie PA
Third party review
No

Clearances, product code FSY

Trailing 12 months

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

FDA records show no clearances under product code FSY in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FSY, 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