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FDA 510(k)

LUMISCOPE ALTERNATING PRESSURE PAD & PUMP

K-Number: K901096 · 1990-08-21

ApplicantLumiscope Co., Inc.
Decision Date1990-08-21
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LUMISCOPE ALTERNATING PRESSURE PAD & PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Lumiscope Co., Inc.. It received FDA 510(k) clearance on 1990-08-21 under 510(k) number K901096. 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 LUMISCOPE ALTERNATING PRESSURE PAD & PUMP?

LUMISCOPE ALTERNATING PRESSURE PAD & PUMP is a medical device that received FDA 510(k) clearance on 1990-08-21. The listed applicant is Lumiscope Co., Inc.. The 510(k) number is K901096.

When did LUMISCOPE ALTERNATING PRESSURE PAD & PUMP receive FDA 510(k) clearance?

LUMISCOPE ALTERNATING PRESSURE PAD & PUMP received FDA 510(k) clearance on 1990-08-21, under 510(k) number K901096.

Who is the listed applicant for LUMISCOPE ALTERNATING PRESSURE PAD & PUMP?

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

What is the FDA product code for LUMISCOPE ALTERNATING PRESSURE PAD & PUMP?

The FDA product code for LUMISCOPE ALTERNATING PRESSURE PAD & PUMP is FNM.

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Other records listing Lumiscope Co., 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.

K032714CARDICARE MODEL MT-301F & MT-301CK954792LUMISCOPE MODEL 2018 THERMOMETERK931768INTERFERENTIAL CURRENT THERAPY UNITK925054INFRARED LAMPK924081LUMISONICK920099GYMMAN

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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.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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