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FDA 510(k)

CONSUMMATE AIR THERAPY BED

K-Number: K890426 · 1989-04-05

ApplicantHealth Products, Inc.
Decision Date1989-04-05
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CONSUMMATE AIR 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 1989-04-05 under 510(k) number K890426. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONSUMMATE AIR THERAPY BED?

CONSUMMATE AIR THERAPY BED is a medical device that received FDA 510(k) clearance on 1989-04-05. The listed applicant is Health Products, Inc.. The 510(k) number is K890426.

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

CONSUMMATE AIR THERAPY BED received FDA 510(k) clearance on 1989-04-05, under 510(k) number K890426.

Who is the listed applicant for CONSUMMATE AIR 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 CONSUMMATE AIR THERAPY BED?

The FDA product code for CONSUMMATE AIR THERAPY BED is FNL.

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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: FNL)

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.

K202964iBed Wireless with iBed MobileStryker CorporationK103536IBED WIRELESS WITH IBED AWARENESSStryker CorporationK982783VAIL 1000 ENCLOSED BEDVail Products, Inc.K974296MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BEDInvacare Corp.K974254BENEFIT B3--- SERIESM.C. Healthcare Products, Inc.K972115VOLKER HOSPITAL BED, MODEL K960Volker Healthcare, 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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