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

CONDUCTIVITY GEL

K Number: K872045 · Decision Jul 15, 1987
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
68
Applicant Total
17
Review Days
49

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Basic Information

Device Name
CONDUCTIVITY GEL
K Number
K872045
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1275
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Futuremed Div. of Future Impex Corp.
Date Received
May 27, 1987
Decision Date
July 15, 1987
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

Similar 510(k) Clearances

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Other Clearances by Futuremed Div. of Future Impex Corp.

K Number Device Name
K933511 UPGRADED SPIROMETER ST-90
K933220 SELECTOR SL 01
K933222 AUDIOMETER DA 323
K903017 MEGA-TENS DUAL CHANNEL T.E.N.S.
K901308 SPIRO ANALYZER MODEL ST 250
K884972 TRANSCOUTANEOUS ELECTRO-NEURO STIMULATOR
K871421 MODEL HL-100 PORTABLE DC ELECT. THERAPEUTIC UNIT
K873817 SPIRO ANALYZER ST-300
K872044 CARBON ELECTRODE
K871913 CONDUCTIVITY GEL
Search all 17 clearances from Futuremed Div. of Future Impex Corp. →