FO51/F151 GOLF MASSAGER

Vibrator, Therapeutic

FAIRFORM MFG., CO., LTD.

The following data is part of a premarket notification filed by Fairform Mfg., Co., Ltd. with the FDA for Fo51/f151 Golf Massager.

Pre-market Notification Details

Device IDK914706
510k NumberK914706
Device Name:FO51/F151 GOLF MASSAGER
ClassificationVibrator, Therapeutic
Applicant FAIRFORM MFG., CO., LTD. 5/F SHING KING INDL. BLDG. 206-208 CHOI HUNG RD. San Po Kong, Kowloon,  HK
ContactWong
CorrespondentWong
FAIRFORM MFG., CO., LTD. 5/F SHING KING INDL. BLDG. 206-208 CHOI HUNG RD. San Po Kong, Kowloon,  HK
Product CodeIRO  
CFR Regulation Number890.5975 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1991-10-18
Decision Date1991-12-09

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