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FDA 510(k)

DISPOSABLE CONTROLLED DROP PASTEUR PIPET

K-Number: K780237 · 1978-03-09

ApplicantOwens-Illinois, Inc.
Decision Date1978-03-09
Product CodeGJG
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE CONTROLLED DROP PASTEUR PIPET is the device name listed in this FDA 510(k) record. The listed applicant is Owens-Illinois, Inc.. It received FDA 510(k) clearance on 1978-03-09 under 510(k) number K780237. 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 DISPOSABLE CONTROLLED DROP PASTEUR PIPET?

DISPOSABLE CONTROLLED DROP PASTEUR PIPET is a medical device that received FDA 510(k) clearance on 1978-03-09. The listed applicant is Owens-Illinois, Inc.. The 510(k) number is K780237.

When did DISPOSABLE CONTROLLED DROP PASTEUR PIPET receive FDA 510(k) clearance?

DISPOSABLE CONTROLLED DROP PASTEUR PIPET received FDA 510(k) clearance on 1978-03-09, under 510(k) number K780237.

Who is the listed applicant for DISPOSABLE CONTROLLED DROP PASTEUR PIPET?

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

What is the FDA product code for DISPOSABLE CONTROLLED DROP PASTEUR PIPET?

The FDA product code for DISPOSABLE CONTROLLED DROP PASTEUR PIPET 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 GroupK781891PIPETTES, PLASTIC DISPOSABLEHillwood Corp.K760719UNIFORM DROP SIZE PASTEUR TYPE PIPETSDade, Baxter Travenol Diagnostics, 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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