510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K073537Substantially Equivalent

Neonatal Bilirubin on Rapidlab Models 1245 and 1265

Siemens Healthcare Diagnostics Inc., Norowood MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K073537 is the FDA 510(k) clearance record for NEONATAL BILIRUBIN ON RAPIDLAB MODELS 1245 AND 1265, a class I device, cleared for Siemens Medical Solutions Diagnostics on under FDA product code MQM (Bilirubin (Total And Unbound) In The Neonate Test System). FDA records list 1,204 510(k) clearances for Siemens Healthcare Diagnostics Inc., from to . As of , FDA records show 7 recalls naming K073537.

Clearance record

Decision date
Received
(193 days to decision)
Product code
MQM Bilirubin (Total And Unbound) In The Neonate Test System
Regulation
21 CFR 862.1113
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Siemens Medical Solutions Diagnostics 2 Edgewater Dr., Norowood MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MQM

Trailing 12 months

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

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