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

PORTABLE ASPIRATOR

K Number: K791210 · Decision Jul 24, 1979
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
76
Applicant Total
1
Review Days
22

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
PORTABLE ASPIRATOR
K Number
K791210
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4780
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Sam Say Assoc.
Date Received
July 2, 1979
Decision Date
July 24, 1979
Product Code
JCX
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
JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JCX), ordered by most recent decision date.

View all