FDA 510(k) FDA class 1 Substantially Equivalent for Some Indications 🇺🇸 United States

SQUEEZE PLAY

K Number: K943730 · Decision Nov 28, 1994
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
64
Applicant Total
29
Review Days
118

Basic Information

Device Name
SQUEEZE PLAY
K Number
K943730
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5975
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent for Some Indications
Applicant
CONAIR CORP.
Date Received
August 2, 1994
Decision Date
November 28, 1994
Product Code
IRO
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
IRO Vibrator, Therapeutic

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K943092 FAMILY FITNESS SHIATSU MASSAGER
K942950 BODY FLEX
K942223 BODY SYSTEM
K940369 BODY RECHARGER
K926339 BODY RELAXER
K911727 INFRADERM; TOUCH 'N TONE PLUS
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