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

DIGITAL ELECTRONIC MYO-GRAPH (MUSCLE ANALYZER)

K Number: K862128 · Decision Jul 11, 1986
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
32
Applicant Total
13
Review Days
37

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Basic Information

Device Name
DIGITAL ELECTRONIC MYO-GRAPH (MUSCLE ANALYZER)
K Number
K862128
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.1500
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Health Products, Inc.
Date Received
June 4, 1986
Decision Date
July 11, 1986
Product Code
KQX
Advisory Committee
Orthopedic
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
KQX Goniometer, Ac-Powered

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Other Clearances by Health Products, Inc.

K Number Device Name
K912866 PEAK EXPIRATORY FLOW METER
K912943 THRESHOLD 2X INSPIRATORY MUSCLE TRAINER
K911807 METERED DOSE INHALER (MDI) SPACER
K902292 MODIFIED ASSESS(R) PEAK FLOW METER
K896953 MODIFIED ASSESS(R) PEAK FLOW METER
K894353 ORTHODERM CONVERTIBLE
K890426 CONSUMMATE AIR THERAPY BED
K874801 ORTHODERM THERAPY BED
K871742 MODIFIED USE OF PLEX INSPIRATORY MUSCLE TRAINER
K870514 THRESHOLD(TM) INSPIRATORY MUSCLE TRAINER
Search all 13 clearances from Health Products, Inc. →