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

OCCUSHIELDS

K Number: K884929 · Decision Dec 15, 1988
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
606
Applicant Total
6
Review Days
17

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Basic Information

Device Name
OCCUSHIELDS
K Number
K884929
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4040
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Dioptics
Date Received
November 28, 1988
Decision Date
December 15, 1988
Product Code
FXX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FXX Mask, Surgical

Similar 510(k) Clearances

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Other Clearances by Dioptics

K Number Device Name
K903487 SOLARSHIELDS ENCORE
K884878 SOLARETTES
K884877 OCUSHIELDS MASKS
K885163 DIOPTICS EYESHIELDS
K862719 SOLARSHIELDS