510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K850268Substantially Equivalent

Sparco Scope Guard

Sparco, Inc., Castro Valley CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K850268 is the FDA 510(k) clearance record for SPARCO SCOPE GUARD, a class II device, cleared for Sparco, Inc. on under FDA product code FEB (Accessories, Cleaning, For Endoscope). FDA's definition for product code FEB reads: "If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at...". FDA records list 6 510(k) clearances for Sparco, Inc., from to . As of , FDA records show no recalls naming K850268.

Clearance record

Decision date
Received
(82 days to decision)
Product code
FEB Accessories, Cleaning, For Endoscope
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Sparco, Inc. P.O. Box 20369, Castro Valley CA
Third party review
No

Clearances, product code FEB

Trailing 12 months

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

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