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FDA 510(k)

ORTHODERM THERAPY BED

K-Number: K874801 · 1988-02-05

ApplicantHealth Products, Inc.
Decision Date1988-02-05
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ORTHODERM THERAPY BED is the device name listed in this FDA 510(k) record. The listed applicant is Health Products, Inc.. It received FDA 510(k) clearance on 1988-02-05 under 510(k) number K874801. The device is classified under product code FNM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHODERM THERAPY BED?

ORTHODERM THERAPY BED is a medical device that received FDA 510(k) clearance on 1988-02-05. The listed applicant is Health Products, Inc.. The 510(k) number is K874801.

When did ORTHODERM THERAPY BED receive FDA 510(k) clearance?

ORTHODERM THERAPY BED received FDA 510(k) clearance on 1988-02-05, under 510(k) number K874801.

Who is the listed applicant for ORTHODERM THERAPY BED?

The FDA 510(k) record lists Health Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ORTHODERM THERAPY BED?

The FDA product code for ORTHODERM THERAPY BED is FNM.

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Other records listing Health Products, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K912866PEAK EXPIRATORY FLOW METERK912943THRESHOLD 2X INSPIRATORY MUSCLE TRAINERK911807METERED DOSE INHALER (MDI) SPACERK902292MODIFIED ASSESS(R) PEAK FLOW METERK896953MODIFIED ASSESS(R) PEAK FLOW METERK894353ORTHODERM CONVERTIBLE

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Related Devices (Code: FNM)

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K973169PRESSURE GUARD SITE SELECT (A)Span-America Medical Systems, Inc.K972022ZAK-2000Cardio Systems, Inc.K974319MIGHTY AIRWheelchairs of KansasK974070PHYSIO/1000Physio Designs, Inc.K972549SIMPULSEKinetic Concepts, Inc.K970081SUPER AIR 9000 ALTERNATING AIR FLOATATION MATTRESS SYSTEMCathay Consolidated, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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