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

CORNING CPF 550 LENS

K Number: K821398 · Decision Jun 25, 1982
Classifications
1
FEI Numbers
602
Registration Numbers
602
Same Product Code
55
Applicant Total
111
Review Days
45

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Basic Information

Device Name
CORNING CPF 550 LENS
K Number
K821398
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.5844
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Corning Medical & Scientific
Date Received
May 11, 1982
Decision Date
June 25, 1982
Product Code
HQG
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
HQG Lens, Spectacle, Non-Custom (Prescription)

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