510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K934254Substantially Equivalent

Impulse 3000 Defibrillator Analyzer

Dynatech/Nevada, Inc., Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K934254 is the FDA 510(k) clearance record for IMPULSE 3000 DEFIBRILLATOR ANALYZER, a class II device, cleared for Dynatech/Nevada, Inc. on under FDA product code DRL (Tester, Defibrillator). FDA records list 6 510(k) clearances for Dynatech/Nevada, Inc., from to . As of , FDA records show no recalls naming K934254.

Clearance record

Decision date
Received
(84 days to decision)
Product code
DRL Tester, Defibrillator
Regulation
21 CFR 870.5325
Device class
Class II
Review panel
Cardiovascular
Applicant
Dynatech/Nevada, Inc. 555 Thirteenth St. NW, Washington DC
510(k) summary
Summary
Third party review
No

Clearances, product code DRL

Trailing 12 months

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

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