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FDA 510(k)

MODEL 4000 ALTERNATING PRESSURE PUMP AND PAD

K-Number: K891259 · 1989-11-17

ApplicantDiamond Medical Equipment, Inc.
Decision Date1989-11-17
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL 4000 ALTERNATING PRESSURE PUMP AND PAD is the device name listed in this FDA 510(k) record. The listed applicant is Diamond Medical Equipment, Inc.. It received FDA 510(k) clearance on 1989-11-17 under 510(k) number K891259. 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 MODEL 4000 ALTERNATING PRESSURE PUMP AND PAD?

MODEL 4000 ALTERNATING PRESSURE PUMP AND PAD is a medical device that received FDA 510(k) clearance on 1989-11-17. The listed applicant is Diamond Medical Equipment, Inc.. The 510(k) number is K891259.

When did MODEL 4000 ALTERNATING PRESSURE PUMP AND PAD receive FDA 510(k) clearance?

MODEL 4000 ALTERNATING PRESSURE PUMP AND PAD received FDA 510(k) clearance on 1989-11-17, under 510(k) number K891259.

Who is the listed applicant for MODEL 4000 ALTERNATING PRESSURE PUMP AND PAD?

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

What is the FDA product code for MODEL 4000 ALTERNATING PRESSURE PUMP AND PAD?

The FDA product code for MODEL 4000 ALTERNATING PRESSURE PUMP AND PAD is FNM.

Related Clinical Trials

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.

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Other records listing Diamond Medical Equipment, 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.

K902520AIR PLUS NEBULIZERK883188T.E.N.S. UNIT SIGMA & TX-3

Related Devices (Code: FNM)

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.

K973169PRESSURE GUARD SITE SELECT (A)Span-America Medical Systems, Inc.K974319MIGHTY AIRWheelchairs of KansasK972022ZAK-2000Cardio Systems, Inc.K974070PHYSIO/1000Physio Designs, Inc.K972549SIMPULSEKinetic Concepts, Inc.K970081SUPER AIR 9000 ALTERNATING AIR FLOATATION MATTRESS SYSTEMCathay Consolidated, Inc.

Official Source

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

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