510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K973973Substantially Equivalent

Elecsys Callcheck Digoxin

Boehringer Mannheim Corp., Pleasanton CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K973973 is the FDA 510(k) clearance record for ELECSYS CALLCHECK DIGOXIN, a class I device, cleared for Boehringer Mannheim Corp. on under FDA product code DMP (Digoxin Control Serum, Ria). FDA records list 340 510(k) clearances for Boehringer Mannheim Corp., from to . As of , FDA records show no recalls naming K973973.

Clearance record

Decision date
Received
(15 days to decision)
Product code
DMP Digoxin Control Serum, Ria
Regulation
21 CFR 862.3280
Device class
Class I
Review panel
Clinical Toxicology
Applicant
Boehringer Mannheim Corp. 4300 Hacienda Dr., Pleasanton CA
510(k) summary
Summary
Third party review
No

Clearances, product code DMP

Trailing 12 months

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

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