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FDA 510(k)

ROLLCHAIR, ORTHO BUCKET SEAT

K-Number: K790560 · 1979-04-10

ApplicantMaddak, Inc.
Decision Date1979-04-10
Product CodeINM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ROLLCHAIR, ORTHO BUCKET SEAT is the device name listed in this FDA 510(k) record. The listed applicant is Maddak, Inc.. It received FDA 510(k) clearance on 1979-04-10 under 510(k) number K790560. The device is classified under product code INM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROLLCHAIR, ORTHO BUCKET SEAT?

ROLLCHAIR, ORTHO BUCKET SEAT is a medical device that received FDA 510(k) clearance on 1979-04-10. The listed applicant is Maddak, Inc.. The 510(k) number is K790560.

When did ROLLCHAIR, ORTHO BUCKET SEAT receive FDA 510(k) clearance?

ROLLCHAIR, ORTHO BUCKET SEAT received FDA 510(k) clearance on 1979-04-10, under 510(k) number K790560.

Who is the listed applicant for ROLLCHAIR, ORTHO BUCKET SEAT?

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

What is the FDA product code for ROLLCHAIR, ORTHO BUCKET SEAT?

The FDA product code for ROLLCHAIR, ORTHO BUCKET SEAT is INM.

Related Clinical Trials

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.

Other records listing Maddak, Inc. 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.

View all 51 devices →

Related Devices (Code: INM)

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.

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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