510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K081879Substantially Equivalent

Spsmedical Sporview Pa Culture Set

Spsmedical Supply Corp., Rush NY / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K081879 is the FDA 510(k) clearance record for SPSMEDICAL SPORVIEW PA CULTURE SET, a class II device, cleared for Spsmedical Supply Corp. on under FDA product code MRB (Indicator, Biological, Liquid Chemical Sterilization Process). FDA records list 28 510(k) clearances for Spsmedical Supply Corp., from to . As of , FDA records show no recalls naming K081879.

Clearance record

Decision date
Received
(28 days to decision)
Product code
MRB Indicator, Biological, Liquid Chemical Sterilization Process
Regulation
21 CFR 880.2800
Device class
Class II
Review panel
General Hospital
Applicant
Spsmedical Supply Corp. 6789 W. Henrietta Rd., Rush NY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MRB

Trailing 12 months

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

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