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FDA 510(k)

MODEL 880 REHABILITATION TRAINER

K-Number: K770234 · 1977-02-14

ApplicantQuinton, Inc.
Decision Date1977-02-14
Product CodeISD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL 880 REHABILITATION TRAINER is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1977-02-14 under 510(k) number K770234. The device is classified under product code ISD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 880 REHABILITATION TRAINER?

MODEL 880 REHABILITATION TRAINER is a medical device that received FDA 510(k) clearance on 1977-02-14. The listed applicant is Quinton, Inc.. The 510(k) number is K770234.

When did MODEL 880 REHABILITATION TRAINER receive FDA 510(k) clearance?

MODEL 880 REHABILITATION TRAINER received FDA 510(k) clearance on 1977-02-14, under 510(k) number K770234.

Who is the listed applicant for MODEL 880 REHABILITATION TRAINER?

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

What is the FDA product code for MODEL 880 REHABILITATION TRAINER?

The FDA product code for MODEL 880 REHABILITATION TRAINER is ISD.

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Other records listing Quinton, Inc. as applicant

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Related Devices (Code: ISD)

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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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