FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

HEARTSTART 3000

K Number: K896919 · Decision May 3, 1990
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
227
Applicant Total
11
Review Days
142

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Basic Information

Device Name
HEARTSTART 3000
K Number
K896919
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.5310
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Laerdal Medical Corp.
Date Received
December 12, 1989
Decision Date
May 3, 1990
Product Code
MKJ
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MKJ Automated External Defibrillators (Non-Wearable)

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Other Clearances by Laerdal Medical Corp.

K Number Device Name
K001742 RESUSCI INFLATE-A-SHIELD CPR BARRIER
K962361 TRACHLIGHT STYLET AND TRACHEAL LIGHTWAND
K954771 TRACHLIGHT STYLET & TRACHEAL LIGHTWAND (ORIGINAL APPLICATION NAME: STYLETT & TRACHEAL LIGHTWAND)
K954609 HEARTSTART 911
K950698 LSU 2000 PORTABLE SUCTION UNIT
K933048 LAERDAL(TM) POCKET MASK, MODIFICATION
K880450 RESUSCI PATIENT FACE SHIELD
K861401 LAERDAL POCKET MASK
K840110 LAERDAL SUCTION UNIT
K822356 MODULAIDE EMERG. CARDIAC LIFE SUPP. KT
Search all 11 clearances from Laerdal Medical Corp. →