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FDA 510(k)

PATIENT BY-PASS

K-Number: K771422 · 1978-01-03

ApplicantQuinton, Inc.
Decision Date1978-01-03
Product CodeFJQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PATIENT BY-PASS is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1978-01-03 under 510(k) number K771422. The device is classified under product code FJQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT BY-PASS?

PATIENT BY-PASS is a medical device that received FDA 510(k) clearance on 1978-01-03. The listed applicant is Quinton, Inc.. The 510(k) number is K771422.

When did PATIENT BY-PASS receive FDA 510(k) clearance?

PATIENT BY-PASS received FDA 510(k) clearance on 1978-01-03, under 510(k) number K771422.

Who is the listed applicant for PATIENT BY-PASS?

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 PATIENT BY-PASS?

The FDA product code for PATIENT BY-PASS is FJQ.

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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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Related Devices (Code: FJQ)

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.

K893679SHUNT CONNECTORSAkcess Medical Products, Inc.K771429DISP. TEFLON CONNHCTORQuinton, Inc.

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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