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FDA 510(k)

MODEL 845T IMAGING/ERGOMETER TABLE

K-Number: K781500 · 1978-09-14

ApplicantQuinton, Inc.
Decision Date1978-09-14
Product CodeJYZ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MODEL 845T IMAGING/ERGOMETER TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1978-09-14 under 510(k) number K781500. The device is classified under product code JYZ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 845T IMAGING/ERGOMETER TABLE?

MODEL 845T IMAGING/ERGOMETER TABLE is a medical device that received FDA 510(k) clearance on 1978-09-14. The listed applicant is Quinton, Inc.. The 510(k) number is K781500.

When did MODEL 845T IMAGING/ERGOMETER TABLE receive FDA 510(k) clearance?

MODEL 845T IMAGING/ERGOMETER TABLE received FDA 510(k) clearance on 1978-09-14, under 510(k) number K781500.

Who is the listed applicant for MODEL 845T IMAGING/ERGOMETER TABLE?

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 845T IMAGING/ERGOMETER TABLE?

The FDA product code for MODEL 845T IMAGING/ERGOMETER TABLE is JYZ.

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Other records listing Quinton, 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.

K032038PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601K021906QUINTON Q-CATH, MODEL 000460K003576Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503K001492QUINTON Q-STRESS, MODEL 000483K992908Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)K990866QUINTON MEDTRACK CR PLUS TREADMILL

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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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