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FDA 510(k)

JAR, COLLECTOR FOR SUCTION SYSTEMS

K-Number: K760333 · 1976-10-27

Decision Date1976-10-27
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

JAR, COLLECTOR FOR SUCTION SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Harris-Lake, Inc.. It received FDA 510(k) clearance on 1976-10-27 under 510(k) number K760333. The device is classified under product code GCX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JAR, COLLECTOR FOR SUCTION SYSTEMS?

JAR, COLLECTOR FOR SUCTION SYSTEMS is a medical device that received FDA 510(k) clearance on 1976-10-27. The listed applicant is Harris-Lake, Inc.. The 510(k) number is K760333.

When did JAR, COLLECTOR FOR SUCTION SYSTEMS receive FDA 510(k) clearance?

JAR, COLLECTOR FOR SUCTION SYSTEMS received FDA 510(k) clearance on 1976-10-27, under 510(k) number K760333.

Who is the listed applicant for JAR, COLLECTOR FOR SUCTION SYSTEMS?

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

What is the FDA product code for JAR, COLLECTOR FOR SUCTION SYSTEMS?

The FDA product code for JAR, COLLECTOR FOR SUCTION SYSTEMS is GCX.

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.

Other records listing Harris-Lake, 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.

View all 7 devices →

Related Devices (Code: GCX)

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

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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