FDA 510(k) Substantially Equivalent 🇺🇸 United States

MINI PULSATOR

K Number: K831474 · Decision Jul 26, 1983
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
4
Review Days
81

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Basic Information

Device Name
MINI PULSATOR
K Number
K831474
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Medelco , Ltd.
Date Received
May 6, 1983
Decision Date
July 26, 1983
Advisory Committee
Unknown
Review Advisory Committee
PM
Third Party
N

Other Clearances by Medelco , Ltd.

K Number Device Name
K853767 FLOSPIK
K831472 ULTRA PULSATOR
K831473 ULTRA PULSATOR MF