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

UNDERPAD, DISPOSABLE POLYPROPY. (UNILUX)

K Number: K760164 · Decision Jul 20, 1976
Classifications
1
FEI Numbers
417
Registration Numbers
418
Same Product Code
55
Applicant Total
47
Review Days
14

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Basic Information

Device Name
UNDERPAD, DISPOSABLE POLYPROPY. (UNILUX)
K Number
K760164
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.5920
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Parke-Davis Co.
Date Received
July 6, 1976
Decision Date
July 20, 1976
Product Code
EYQ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
EYQ Garment, Protective, For Incontinence

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K855120 ATI DISPOSABLE BIOLOGICAL TEST PACK
K860570 ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE
K860290 VIAPIC CENTRAL LINE CATHETER
K852192 DISPOSABLE STEAM BIOLOGICAL TEST PACK
K841967 DESERET THERMODILUTION CARDIAC OUTPUT
K851327 DESERET ARTERIAL CATHETER
K852078 SPECTRUM(TENTATIVE)
K844840 DESERET INTRODUCER SET
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