FDA 510(k)

DISC-O-AID

K-Number: K821903 · 1982-07-20

Decision Date1982-07-20

Product CodeIKX

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

DISC-O-AID is the device name listed in this FDA 510(k) record. The listed applicant is M. Dahm International Aps. It received FDA 510(k) clearance on 1982-07-20 under 510(k) number K821903. The device is classified under product code IKX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISC-O-AID?

DISC-O-AID is a medical device that received FDA 510(k) clearance on 1982-07-20. The listed applicant is M. Dahm International Aps. The 510(k) number is K821903.

When did DISC-O-AID receive FDA 510(k) clearance?

DISC-O-AID received FDA 510(k) clearance on 1982-07-20, under 510(k) number K821903.

Who is the listed applicant for DISC-O-AID?

The FDA 510(k) record lists M. Dahm International Aps as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISC-O-AID?

The FDA product code for DISC-O-AID is IKX.

Related Devices (Code: IKX)

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.

K862895TRICYCLESMednet, Inc.K842650WALL GRAB BARS 98130-98136Guardian Products Co., Inc.K831541TUB TRANSFER BENCH BK6481Fred Sammons, Inc.K823640BATH TUB SAFETY BARFred Sammons, Inc.K823639BOARD TO TRANSFER PARALYZED PATIENT FROMFred Sammons, Inc.K823634CHAIR OR BED LEG EXTENDERSFred Sammons, 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.