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FDA 510(k)

CLINITRON AIR FLUIDIZED SUPPORT J-101UD

K-Number: K843389 · 1984-09-05

ApplicantUhi Corp.
Decision Date1984-09-05
Product CodeINX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CLINITRON AIR FLUIDIZED SUPPORT J-101UD is the device name listed in this FDA 510(k) record. The listed applicant is Uhi Corp.. It received FDA 510(k) clearance on 1984-09-05 under 510(k) number K843389. 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 CLINITRON AIR FLUIDIZED SUPPORT J-101UD?

CLINITRON AIR FLUIDIZED SUPPORT J-101UD is a medical device that received FDA 510(k) clearance on 1984-09-05. The listed applicant is Uhi Corp.. The 510(k) number is K843389.

When did CLINITRON AIR FLUIDIZED SUPPORT J-101UD receive FDA 510(k) clearance?

CLINITRON AIR FLUIDIZED SUPPORT J-101UD received FDA 510(k) clearance on 1984-09-05, under 510(k) number K843389.

Who is the listed applicant for CLINITRON AIR FLUIDIZED SUPPORT J-101UD?

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

What is the FDA product code for CLINITRON AIR FLUIDIZED SUPPORT J-101UD?

The FDA product code for CLINITRON AIR FLUIDIZED SUPPORT J-101UD is INX.

Related Clinical Trials

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Other records listing Uhi Corp. 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.

K821835BARRIER BURN SHEETK813584CLINITRON AIR FLUIDIZED SUPPORT SYSTEM

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

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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