510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K071591Substantially Equivalent

Ramp Influenza A/b Assay

Response Biomedical Corp., Burnaby, British Columbia, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K071591 is the FDA 510(k) clearance record for RAMP INFLUENZA A/B ASSAY, a class II device, cleared for Response Biomedical Corp. on under FDA product code PSZ (Devices Detecting Influenza A, B, And C Virus Antigens). FDA's definition for product code PSZ reads: "An influenza virus antigen detection test system is a device intended for the qualitative detection of influenza viral antigens directly from clinical specimens in patients with signs and symptoms of respiratory infection". FDA records list 7 510(k) clearances for Response Biomedical Corp., from to . As of , FDA records show no recalls naming K071591.

Clearance record

Decision date
Received
(310 days to decision)
Product code
PSZ Devices Detecting Influenza A, B, And C Virus Antigens
Regulation
21 CFR 866.3328
Device class
Class II
Review panel
Microbiology
Applicant
Response Biomedical Corp. 100 - 8900 Glenlyon Pkwy., Burnaby, British Columbia, CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code PSZ

Trailing 12 months
2 clearances under product code PSZ in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code PSZ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20261
October 20260