Atlas FDA

TWEEZER-TYPE EPILATOR

FDA 510(k) clearance K970338 · decided 1997-07-01

Clearance details

K-number
K970338
Device name
TWEEZER-TYPE EPILATOR
Applicant
Igia Direct, Inc.
Decision
Substantially Equivalent
Date received
1997-01-29
Decision date
1997-07-01
Days to decision
153 days
Clearance type
Traditional
Product code
KCX
Device class
1
Regulation number
878.5360
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Westford, MA, 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
DAPELLE HAIR REMOVER (K973773)Wellquest Intl., Inc.1997-12-17
TWEEZER-TYPE EPILATOR (K973340)Mobit, Inc.1997-12-03
SONIQUE HAIR REMOVER (K973174)Global TV Concepts, Ltd.1997-10-30
FEMINIQUE SONIC HAIR REMOVER (K973179)Global TV Concepts, Ltd.1997-10-30
FINALLY FREE (K972695)Mehl/Group Marketing1997-10-22
EPI 2 (K935706)Universal H.R. System, Inc.1997-02-11
COMMANDER MARK II HAIR REMOVAL SYSTEM (K943872)The Helene Edgar Corp.1995-10-26
EPILATOR (K952117)Burke Neutech, Inc.1995-10-19
HAIR TRONICS MODEL HT8000 (K915845)Global Tronics Intl., Inc.1992-07-29
GUARANTY HAIR REMOVAL SYSTEM (K905125)Stephens Mfg. Co.1991-08-05
AHRS EPILATOR 629 (K892514)American Hair Removal System Co.1990-08-14
EPILATOR 8500 (K851413)Lois Yee Cosmetics, Inc.1985-06-10

Recalls involving this device

No recalls on record reference this clearance.