510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K012040Substantially Equivalent

Ramp Myoglobin Assay

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

K012040 is the FDA 510(k) clearance record for RAMP MYOGLOBIN ASSAY, a class II device, cleared for Response Biomedical Corp. on under FDA product code DDR (Myoglobin, Antigen, Antiserum, Control). FDA records list 7 510(k) clearances for Response Biomedical Corp., from to . As of , FDA records show no recalls naming K012040.

Clearance record

Decision date
Received
(172 days to decision)
Product code
DDR Myoglobin, Antigen, Antiserum, Control
Regulation
21 CFR 866.5680
Device class
Class II
Review panel
Immunology
Applicant
Response Biomedical Corp. 8855 Northbrook Ct., Burnaby, British Columbia, CA
510(k) summary
Summary
Third party review
No

Clearances, product code DDR

Trailing 12 months

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

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