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FDA 510(k)

BUSHLINE CARE CHAIR

K-Number: K880786 · 1988-03-14

Decision Date1988-03-14
Product CodeINO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BUSHLINE CARE CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Bushline Corp.. It received FDA 510(k) clearance on 1988-03-14 under 510(k) number K880786. The device is classified under product code INO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BUSHLINE CARE CHAIR?

BUSHLINE CARE CHAIR is a medical device that received FDA 510(k) clearance on 1988-03-14. The listed applicant is Bushline Corp.. The 510(k) number is K880786.

When did BUSHLINE CARE CHAIR receive FDA 510(k) clearance?

BUSHLINE CARE CHAIR received FDA 510(k) clearance on 1988-03-14, under 510(k) number K880786.

Who is the listed applicant for BUSHLINE CARE CHAIR?

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

What is the FDA product code for BUSHLINE CARE CHAIR?

The FDA product code for BUSHLINE CARE CHAIR is INO.

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.

Related Devices (Code: INO)

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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