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

ORTHODERM CONVERTIBLE

K Number: K894353 · Decision Aug 9, 1989
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
56
Applicant Total
13
Review Days
26

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Basic Information

Device Name
ORTHODERM CONVERTIBLE
K Number
K894353
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5170
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Health Products, Inc.
Date Received
July 14, 1989
Decision Date
August 9, 1989
Product Code
IOQ
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
IOQ Bed, Flotation Therapy, 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
K890426 CONSUMMATE AIR THERAPY BED
K874801 ORTHODERM THERAPY BED
K871742 MODIFIED USE OF PLEX INSPIRATORY MUSCLE TRAINER
K870514 THRESHOLD(TM) INSPIRATORY MUSCLE TRAINER
K864719 PFLEX EM(TM) (EXERCISE MONITOR)
Search all 13 clearances from Health Products, Inc. →