Atlas FDA

SPECTACLE FRAME

FDA 510(k) clearance K945323 · decided 1994-11-22

Clearance details

K-number
K945323
Device name
SPECTACLE FRAME
Applicant
M.Y. Vision Corp.
Decision
Substantially Equivalent
Date received
1994-11-01
Decision date
1994-11-22
Days to decision
21 days
Clearance type
Traditional
Product code
HQZ
Device class
1
Regulation number
886.5842
Medical specialty
Ophthalmic
Advisory committee
Ophthalmic
Location
Paramus, NJ, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
VIEW POINT, DORION, RUDDY PROJECT, ULTRA FLEX, TRILLON, BAY BOY, SHIELD SKI, SUN POCKETS, POINT OF VIEW (K952597)Point of View Optical Outlet, Inc.1995-09-12
SPECTACLE FRAME (K944313)Sun Hing Optical Manufactory , Ltd.1995-03-28
SPECTACLE FRAME (K945392)Seo Han Corp., Ltd.1994-12-15
SPECTACLE FRAME OR EYEGLASS FRAMES (K945176)Optipia Trading Co.1994-12-15
OPTICAL FRAMES (K945770)Ramada Optics, Inc.1994-12-15
FRAME, SPECTACLES (K945350)Taiwan Eva Industrial Co., Inc.1994-12-13
MAG-1 SPECTACLE FRAME (K945342)Criss Optical Mfg. Co., Inc.1994-11-28
ARISTAR EYEWEAR, ESPRIT EYEWEAR (K945123)Aristar Inc. U.S.A.1994-11-22
SPECTACLE FRAMES OR EYEGLASS FRAMES (K945340)Mi Mun Corp.1994-11-22
FRAME, SPECTACLE (K945450)Kookje Apis Industrial Co.1994-11-22
NIL (K944641)Max-Vision (H.K.)Limited1994-11-14
SPECTACLE FRAMES (K944373)Custom Optical Frames, Inc.1994-09-28

Recalls involving this device

No recalls on record reference this clearance.