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FDA 510(k)

PIPETTES, PLASTIC DISPOSABLE

K-Number: K781891 · 1978-11-15

ApplicantHillwood Corp.
Decision Date1978-11-15
Product CodeGJG
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

PIPETTES, PLASTIC DISPOSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Hillwood Corp.. It received FDA 510(k) clearance on 1978-11-15 under 510(k) number K781891. 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 PIPETTES, PLASTIC DISPOSABLE?

PIPETTES, PLASTIC DISPOSABLE is a medical device that received FDA 510(k) clearance on 1978-11-15. The listed applicant is Hillwood Corp.. The 510(k) number is K781891.

When did PIPETTES, PLASTIC DISPOSABLE receive FDA 510(k) clearance?

PIPETTES, PLASTIC DISPOSABLE received FDA 510(k) clearance on 1978-11-15, under 510(k) number K781891.

Who is the listed applicant for PIPETTES, PLASTIC DISPOSABLE?

The FDA 510(k) record lists Hillwood Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PIPETTES, PLASTIC DISPOSABLE?

The FDA product code for PIPETTES, PLASTIC DISPOSABLE is GJG.

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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.

K831079LIQUIPETTEThe Kendall Company Div. of Tyco Healthcare GroupK780237DISPOSABLE 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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