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FDA 510(k)

LAKE STAGEZERO(TM) AIR FLOTATION BED

K-Number: K943162 · 1995-02-27

ApplicantLake Medical Products, Inc.
Decision Date1995-02-27
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LAKE STAGEZERO(TM) AIR FLOTATION BED is the device name listed in this FDA 510(k) record. The listed applicant is Lake Medical Products, Inc.. It received FDA 510(k) clearance on 1995-02-27 under 510(k) number K943162. 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 LAKE STAGEZERO(TM) AIR FLOTATION BED?

LAKE STAGEZERO(TM) AIR FLOTATION BED is a medical device that received FDA 510(k) clearance on 1995-02-27. The listed applicant is Lake Medical Products, Inc.. The 510(k) number is K943162.

When did LAKE STAGEZERO(TM) AIR FLOTATION BED receive FDA 510(k) clearance?

LAKE STAGEZERO(TM) AIR FLOTATION BED received FDA 510(k) clearance on 1995-02-27, under 510(k) number K943162.

Who is the listed applicant for LAKE STAGEZERO(TM) AIR FLOTATION BED?

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

What is the FDA product code for LAKE STAGEZERO(TM) AIR FLOTATION BED?

The FDA product code for LAKE STAGEZERO(TM) AIR FLOTATION BED 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Lake Medical 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.

K922730LAKE OSTOMY CARE SETK905053STAGE ZERO AIR FLOTATION BEDK901835LAKE N/G FEEDING TUBE (WITH Y PORT CONNECTOR)K902508LAKE MALE EXTERNAL CATHETERIZATION KITK902121LAKE GASTROSTOMY TUBEK884127LAKE N/G FEEDING TUBE

View all 15 devices →

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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