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FDA 510(k)

APOLLO AIR FLUIDIZED BED

K-Number: K842987 · 1984-08-02

ApplicantApollo Fluid Dynamics
Decision Date1984-08-02
Product CodeINX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

APOLLO AIR FLUIDIZED BED is the device name listed in this FDA 510(k) record. The listed applicant is Apollo Fluid Dynamics. It received FDA 510(k) clearance on 1984-08-02 under 510(k) number K842987. The device is classified under product code INX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APOLLO AIR FLUIDIZED BED?

APOLLO AIR FLUIDIZED BED is a medical device that received FDA 510(k) clearance on 1984-08-02. The listed applicant is Apollo Fluid Dynamics. The 510(k) number is K842987.

When did APOLLO AIR FLUIDIZED BED receive FDA 510(k) clearance?

APOLLO AIR FLUIDIZED BED received FDA 510(k) clearance on 1984-08-02, under 510(k) number K842987.

Who is the listed applicant for APOLLO AIR FLUIDIZED BED?

The FDA 510(k) record lists Apollo Fluid Dynamics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for APOLLO AIR FLUIDIZED BED?

The FDA product code for APOLLO AIR FLUIDIZED BED is INX.

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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Related Devices (Code: INX)

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.

K972176HOME CARE BEAD BEDKinetic Concepts, Inc.K964223CLINITRON RITE-HITEHill-Rom, Inc.K943385CLINITRON ELEXISSsi Medical Services, Inc.K942184CLINITRON AT HOME AIR FLUIDED THERAPYSsi Medical Services, Inc.K931168X-20 AIR SUPPORT BEDAmerican Life Support Technology, Inc.K934689LOW AIR LOSS MATTRESS, MODIFICATIONCardio Systems, 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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