510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K902359Substantially Equivalent

Surgical Video Camera, Model 9500

Seitz Technical Products, Inc., Doylestown PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902359 is the FDA 510(k) clearance record for SURGICAL VIDEO CAMERA, MODEL 9500, a class I device, cleared for Seitz Technical Products, Inc. on under FDA product code FWB (Camera, Television, Surgical, Without Audio). FDA records list one 510(k) clearance for Seitz Technical Products, Inc. As of , FDA records show no recalls naming K902359.

Clearance record

Decision date
Received
(44 days to decision)
Product code
FWB Camera, Television, Surgical, Without Audio
Regulation
21 CFR 878.4160
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Seitz Technical Products, Inc. 187 E. Ashland St., Doylestown PA
Third party review
No

Clearances, product code FWB

Trailing 12 months

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

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