Atlas FDA

FITO DIDO

FDA 510(k) clearance K963075 · decided 1996-08-22

Clearance details

K-number
K963075
Device name
FITO DIDO
Applicant
Framesmart, Inc.
Decision
Substantially Equivalent
Date received
1996-07-24
Decision date
1996-08-22
Days to decision
29 days
Clearance type
Traditional
Product code
HQY
Device class
1
Regulation number
886.5850
Medical specialty
Ophthalmic
Advisory committee
Ophthalmic
Location
Miami, FL, 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
NON-PRESCRIPTION SUNGLASSES (K974860)Wenzhou Ming Ming Optical Co. , Ltd.1998-01-30
NON-PRESCRIPTION SUNGLASSES (K974852)Chia Hui Spectacles Mfg. Corp.1998-01-30
NON-PRESCRIPTION SUNGLASSES (K974861)Wenzhou Hindar Optical Co., Ltd.1998-01-27
SUNGLASSES (K974511)Sun World Intl., Inc.1998-01-12
SUNGLASSES (K974441)Hip Shing Fat Co., Ltd.1998-01-09
MULTI (K974414)Morning Calm Corp.1997-12-08
SUNGLASSES (K973528)Jeou Jeou Long Industrial Co., Ltd.1997-12-08
NON-PRESCRIPTION SUNGLASSES (K974179)Taipan Optical Company , Ltd.1997-12-01
VENNETO (K974045)Amsure Sports, Inc.1997-11-20
SUNGLASSES (K973934)Elegance Optical Manufactory, Ltd.1997-11-18
SUNGLASSES (K973526)Pyramid Handbags, Inc.1997-10-16
SUNGLASSES (K973490)Tong Yang Optical Co.1997-09-30

Recalls involving this device

No recalls on record reference this clearance.