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FDA 510(k)

STAGE ZERO AIR FLOTATION BED

K-Number: K905053 · 1990-11-26

ApplicantLake Medical Products, Inc.
Decision Date1990-11-26
Product CodeIOQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STAGE ZERO 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 1990-11-26 under 510(k) number K905053. The device is classified under product code IOQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAGE ZERO AIR FLOTATION BED?

STAGE ZERO AIR FLOTATION BED is a medical device that received FDA 510(k) clearance on 1990-11-26. The listed applicant is Lake Medical Products, Inc.. The 510(k) number is K905053.

When did STAGE ZERO AIR FLOTATION BED receive FDA 510(k) clearance?

STAGE ZERO AIR FLOTATION BED received FDA 510(k) clearance on 1990-11-26, under 510(k) number K905053.

Who is the listed applicant for STAGE ZERO 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 STAGE ZERO AIR FLOTATION BED?

The FDA product code for STAGE ZERO AIR FLOTATION BED is IOQ.

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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.

K943162LAKE STAGEZERO(TM) AIR FLOTATION BEDK922730LAKE OSTOMY CARE SETK901835LAKE N/G FEEDING TUBE (WITH Y PORT CONNECTOR)K902508LAKE MALE EXTERNAL CATHETERIZATION KITK902121LAKE GASTROSTOMY TUBEK884127LAKE N/G FEEDING TUBE

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Related Devices (Code: IOQ)

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.

K122473TOTALCARE SPOT TOTALCARE BARIATRIC TOTALCARE DUO TOATALCARE BED SYSTEM TOTALCARE DUO2Hill-RomK973624NURSE'S AID PATIENT ROTATION SYSTEMAir Med Assist ProductsK970363HYDROTEC LOW AIR LOSS THERAPY BEDApex Metal, Inc.K970364AIRTEC2 LOW AIR LOSS THERAPY BEDApex Metal, Inc.K970636TOTALCARE., MODULAR THERAPY SYSTEM (MTS)Hill-Rom, Inc.K964873SILKAIR LOW AIRLOSS THERAPYHill-Rom, 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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