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FDA 510(k)

RINSE BLOCK CONNECTOR

K-Number: K771482 · 1978-01-03

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

Device Summary

RINSE BLOCK CONNECTOR 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 K771482. The device is classified under product code KDJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RINSE BLOCK CONNECTOR?

RINSE BLOCK CONNECTOR 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 K771482.

When did RINSE BLOCK CONNECTOR receive FDA 510(k) clearance?

RINSE BLOCK CONNECTOR received FDA 510(k) clearance on 1978-01-03, under 510(k) number K771482.

Who is the listed applicant for RINSE BLOCK CONNECTOR?

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 RINSE BLOCK CONNECTOR?

The FDA product code for RINSE BLOCK CONNECTOR is KDJ.

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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.

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Related Devices (Code: KDJ)

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.

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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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