FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ZEE ELECTRODE-GEL

K Number: K812284 · Decision Sep 8, 1981
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
68
Applicant Total
8
Review Days
26

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Basic Information

Device Name
ZEE ELECTRODE-GEL
K Number
K812284
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1275
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Zee Medical Products Co., Inc.
Date Received
August 13, 1981
Decision Date
September 8, 1981
Product Code
GYB
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GYB Media, Electroconductive

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Other Clearances by Zee Medical Products Co., Inc.

K Number Device Name
K823501 ZEE SPHYGMOMANOMETER
K813156 ULTRA-WIDE SAFETY SPECTACLE FRAME
K813016 ZEE TRACTION SPLINT
K812814 ZEE SURGICAL INSTRUMENTS
K812564 ZEE LIFE SUPPORT AIR PANTS
K812342 ZEE EXTRICATION DEVICE
K812022 ZEE MANUAL RESUSCITATOR