510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K832833Substantially Equivalent

Personal Defibrillator

Physio Control, Inc., Redmond WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K832833 is the FDA 510(k) clearance record for PERSONAL DEFIBRILLATOR, a class II device, cleared for Physio-Control, Inc. on under FDA product code LDD (Dc-Defibrillator, Low-Energy, (Including Paddles)). FDA records list 108 510(k) clearances for Physio-Control, Inc., from to . As of , FDA records show no recalls naming K832833.

Clearance record

Decision date
Received
(434 days to decision)
Product code
LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
Regulation
21 CFR 870.5300
Device class
Class II
Review panel
Cardiovascular
Applicant
Physio-Control, Inc. 11811 Willows Rd. NE, P.O. Box 97006, Redmond WA
Third party review
No

Clearances, product code LDD

Trailing 12 months

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

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