510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K051779Substantially Equivalent

Androflow - Respiratory Rate Monitor

Andromed, Inc., Saint Laurent, Quebec, CA / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)

K051779 is the FDA 510(k) clearance record for ANDROFLOW - RESPIRATORY RATE MONITOR, a class II device, cleared for Andromed, Inc. on under FDA product code BZQ (Monitor, Breathing Frequency). FDA records list 5 510(k) clearances for Andromed, Inc., from to . As of , FDA records show no recalls naming K051779.

Clearance record

Decision date
Received
(91 days to decision)
Product code
BZQ Monitor, Breathing Frequency
Regulation
21 CFR 868.2375
Device class
Class II
Review panel
Anesthesiology
Applicant
Andromed, Inc. 4610 Chemin Du Bois-Franc, Saint Laurent, Quebec, CA
510(k) summary
Statement
Third party review
No

Clearances, product code BZQ

Trailing 12 months
2 clearances under product code BZQ in the twelve months to October 2026, June 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code BZQ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20262
July 20260
August 20260
September 20260
October 20260