510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K901559Substantially Equivalent

Modification to Api Uniscept 20Gp

Analytical Products, Inc., Plainview NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K901559 is the FDA 510(k) clearance record for MODIFICATION TO API UNISCEPT 20GP, a class I device, cleared for Analytical Products, Inc. on under FDA product code LQL (Gram Positive Identification Panel). FDA records list 57 510(k) clearances for Analytical Products, Inc., from to . As of , FDA records show no recalls naming K901559.

Clearance record

Decision date
Received
(160 days to decision)
Product code
LQL Gram Positive Identification Panel
Regulation
21 CFR 866.2660
Device class
Class I
Review panel
Microbiology
Applicant
Analytical Products, Inc. 200 Express St., Plainview NY
Third party review
No

Clearances, product code LQL

Trailing 12 months

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

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