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FDA 510(k)

X-20 AIR SUPPORT BED

K-Number: K931168 · 1994-02-17

ApplicantAmerican Life Support Technology, Inc.
Decision Date1994-02-17
Product CodeINX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

X-20 AIR SUPPORT BED is the device name listed in this FDA 510(k) record. The listed applicant is American Life Support Technology, Inc.. It received FDA 510(k) clearance on 1994-02-17 under 510(k) number K931168. 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 X-20 AIR SUPPORT BED?

X-20 AIR SUPPORT BED is a medical device that received FDA 510(k) clearance on 1994-02-17. The listed applicant is American Life Support Technology, Inc.. The 510(k) number is K931168.

When did X-20 AIR SUPPORT BED receive FDA 510(k) clearance?

X-20 AIR SUPPORT BED received FDA 510(k) clearance on 1994-02-17, under 510(k) number K931168.

Who is the listed applicant for X-20 AIR SUPPORT BED?

The FDA 510(k) record lists American Life Support Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for X-20 AIR SUPPORT BED?

The FDA product code for X-20 AIR SUPPORT BED is INX.

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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.K934689LOW AIR LOSS MATTRESS, MODIFICATIONCardio Systems, Inc.K924973DYLNAMEDICS A.S.A.P.Dynamedics, 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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