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FDA 510(k)

MEDISCUS AIR BED

K-Number: K760712 · 1976-11-24

ApplicantHsi Products, Inc.
Decision Date1976-11-24
Product CodeINX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MEDISCUS AIR BED is the device name listed in this FDA 510(k) record. The listed applicant is Hsi Products, Inc.. It received FDA 510(k) clearance on 1976-11-24 under 510(k) number K760712. 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 MEDISCUS AIR BED?

MEDISCUS AIR BED is a medical device that received FDA 510(k) clearance on 1976-11-24. The listed applicant is Hsi Products, Inc.. The 510(k) number is K760712.

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

MEDISCUS AIR BED received FDA 510(k) clearance on 1976-11-24, under 510(k) number K760712.

Who is the listed applicant for MEDISCUS AIR BED?

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

What is the FDA product code for MEDISCUS AIR BED?

The FDA product code for MEDISCUS AIR BED is INX.

Related Clinical Trials

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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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