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FDA 510(k)

LIQUIPETTE

K-Number: K831079 · 1983-04-28

ApplicantThe Kendall Company Div. of Tyco Healthcare Group
Decision Date1983-04-28
Product CodeGJG
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

LIQUIPETTE is the device name listed in this FDA 510(k) record. The listed applicant is The Kendall Company Div. of Tyco Healthcare Group. It received FDA 510(k) clearance on 1983-04-28 under 510(k) number K831079. The device is classified under product code GJG. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUIPETTE?

LIQUIPETTE is a medical device that received FDA 510(k) clearance on 1983-04-28. The listed applicant is The Kendall Company Div. of Tyco Healthcare Group. The 510(k) number is K831079.

When did LIQUIPETTE receive FDA 510(k) clearance?

LIQUIPETTE received FDA 510(k) clearance on 1983-04-28, under 510(k) number K831079.

Who is the listed applicant for LIQUIPETTE?

The FDA 510(k) record lists The Kendall Company Div. of Tyco Healthcare Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIQUIPETTE?

The FDA product code for LIQUIPETTE is GJG.

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.

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Other records listing The Kendall Company Div. of Tyco Healthcare Group 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.

K024010DOVER SILVER HYDROGEL COATED SILICONE FOLEY CATHETERK831081EZEE FILTER/SEPARATORK831082CONNECTING TUBING

Related Devices (Code: GJG)

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.

K781891PIPETTES, PLASTIC DISPOSABLEHillwood Corp.K780237DISPOSABLE CONTROLLED DROP PASTEUR PIPETOwens-Illinois, Inc.K760719UNIFORM DROP SIZE PASTEUR TYPE PIPETSDade, Baxter Travenol Diagnostics, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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