FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

AEROSOL MASK

K Number: K770995 · Decision Jun 27, 1977
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
54
Applicant Total
47
Review Days
26

Basic Information

Device Name
AEROSOL MASK
K Number
K770995
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5580
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
OHIO MEDICAL PRODUCTS
Date Received
June 1, 1977
Decision Date
June 27, 1977
Product Code
BYG
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BYG Mask, Oxygen

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