510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K955085Substantially Equivalent

Hm-Cap Eia Test (Modification)

Schiff & Co., West Cadwell NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K955085 is the FDA 510(k) clearance record for HM-CAP EIA TEST (MODIFICATION), a class I device, cleared for Schiff & Co. on under FDA product code LYR (Helicobacter Pylori). FDA records list 15 510(k) clearances for Schiff & Co., from to . As of , FDA records show no recalls naming K955085.

Clearance record

Decision date
Received
(106 days to decision)
Product code
LYR Helicobacter Pylori
Regulation
21 CFR 866.3110
Device class
Class I
Review panel
Microbiology
Applicant
Schiff & Co. 1129 Bloomfield Ave., West Cadwell NJ
510(k) summary
Statement
Third party review
No

Clearances, product code LYR

Trailing 12 months

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

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