FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

LAERDAL SUCTION UNIT

K Number: K840110 · Decision Mar 12, 1984
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
158
Applicant Total
11
Review Days
62

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Basic Information

Device Name
LAERDAL SUCTION UNIT
K Number
K840110
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4780
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Laerdal Medical Corp.
Date Received
January 10, 1984
Decision Date
March 12, 1984
Product Code
BTA
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
BTA Pump, Portable, Aspiration (Manual Or Powered)

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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
K896919 HEARTSTART 3000
K880450 RESUSCI PATIENT FACE SHIELD
K861401 LAERDAL POCKET MASK
K822356 MODULAIDE EMERG. CARDIAC LIFE SUPP. KT
Search all 11 clearances from Laerdal Medical Corp. →