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

PRENATAL SUPPORT PILLOW

K Number: K810035 · Decision Jan 23, 1981
Classifications
1
FEI Numbers
279
Registration Numbers
280
Same Product Code
7
Applicant Total
1
Review Days
14

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Basic Information

Device Name
PRENATAL SUPPORT PILLOW
K Number
K810035
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.6820
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Supportech, Inc.
Date Received
January 9, 1981
Decision Date
January 23, 1981
Product Code
CCX
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
CCX Support, Patient Position

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