510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K770614Substantially Equivalent

Monitor, Gas Manifold

Dynatech Cryomedical Co., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K770614 is the FDA 510(k) clearance record for MONITOR, GAS MANIFOLD, a class I device, cleared for Dynatech Cryomedical Co. on under FDA product code BXH (Gauge, Gas Pressure, Cylinder/Pipeline). FDA records list 6 510(k) clearances for Dynatech Cryomedical Co., from to . As of , FDA records show no recalls naming K770614.

Clearance record

Decision date
Received
(7 days to decision)
Product code
BXH Gauge, Gas Pressure, Cylinder/Pipeline
Regulation
21 CFR 868.2610
Device class
Class I
Review panel
Anesthesiology
Applicant
Dynatech Cryomedical Co. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code BXH

Trailing 12 months

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

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