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FDA 510(k)

NEW SUPPORT SYS. FOR BEDRIDDEN PATIENTS

K-Number: K821185 · 1982-09-14

ApplicantDase Co.
Decision Date1982-09-14
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NEW SUPPORT SYS. FOR BEDRIDDEN PATIENTS is the device name listed in this FDA 510(k) record. The listed applicant is Dase Co.. It received FDA 510(k) clearance on 1982-09-14 under 510(k) number K821185. 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 NEW SUPPORT SYS. FOR BEDRIDDEN PATIENTS?

NEW SUPPORT SYS. FOR BEDRIDDEN PATIENTS is a medical device that received FDA 510(k) clearance on 1982-09-14. The listed applicant is Dase Co.. The 510(k) number is K821185.

When did NEW SUPPORT SYS. FOR BEDRIDDEN PATIENTS receive FDA 510(k) clearance?

NEW SUPPORT SYS. FOR BEDRIDDEN PATIENTS received FDA 510(k) clearance on 1982-09-14, under 510(k) number K821185.

Who is the listed applicant for NEW SUPPORT SYS. FOR BEDRIDDEN PATIENTS?

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

What is the FDA product code for NEW SUPPORT SYS. FOR BEDRIDDEN PATIENTS?

The FDA product code for NEW SUPPORT SYS. FOR BEDRIDDEN PATIENTS is FNL.

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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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