510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K870942Substantially Equivalent

Mvs Fiberoptic Lightpipe

Advanced Surgical Products, Inc., Charles MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K870942 is the FDA 510(k) clearance record for MVS FIBEROPTIC LIGHTPIPE, a class II device, cleared for Advanced Surgical Products, Inc. on under FDA product code FST (Light, Surgical, Fiberoptic). FDA records list 64 510(k) clearances for Advanced Surgical Products, Inc., from to . As of , FDA records show no recalls naming K870942.

Clearance record

Decision date
Received
(25 days to decision)
Product code
FST Light, Surgical, Fiberoptic
Regulation
21 CFR 878.4580
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Advanced Surgical Products, Inc. 524 Chele Dr. St., Charles MO
Third party review
No

Clearances, product code FST

Trailing 12 months

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

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