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

NEMECTRON MICROWAVE

K Number: K895000 · Decision Jul 27, 1990
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
3
Applicant Total
13
Review Days
353

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Basic Information

Device Name
NEMECTRON MICROWAVE
K Number
K895000
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5275
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Nemectron Medical, Inc.
Date Received
August 8, 1989
Decision Date
July 27, 1990
Product Code
IOA
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
IOA Diathermy, Microwave, For Use In Applying Therapeutic Deep Heat

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (IOA), ordered by most recent decision date.

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Other Clearances by Nemectron Medical, Inc.

K Number Device Name
K923396 THERMODYN
K862376 NEMECTROSON MODEL 2
K854720 NEMECTRODYN MODEL 2 & ENDOVAC 2 POWER MUSCLE STIM.
K854721 NEMECTRODYN MODEL 2 & ENDOVAC 2
K844416 THERMOPULS E
K843735 SOFTEPIL
K843734 NEMDI
K823511 EMG BIOFEEDBACK DEVICE
K820334 NEMECTRODYN MODELS 8,7,5 (VOLS. I-IV
K810513 ELECTRODYN CII-INTERFERENTIAL MUSCLE
Search all 13 clearances from Nemectron Medical, Inc. →