FDA 510(k)

PIPETS BOROSILICATE GLASS

K-Number: K771138 · 1977-08-04

ApplicantDade, Baxter Travenol Diagnostics, Inc.

Decision Date1977-08-04

Product CodeGJW

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

PIPETS BOROSILICATE GLASS is the device name listed in this FDA 510(k) record. The listed applicant is Dade, Baxter Travenol Diagnostics, Inc.. It received FDA 510(k) clearance on 1977-08-04 under 510(k) number K771138. The device is classified under product code GJW. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIPETS BOROSILICATE GLASS?

PIPETS BOROSILICATE GLASS is a medical device that received FDA 510(k) clearance on 1977-08-04. The listed applicant is Dade, Baxter Travenol Diagnostics, Inc.. The 510(k) number is K771138.

When did PIPETS BOROSILICATE GLASS receive FDA 510(k) clearance?

PIPETS BOROSILICATE GLASS received FDA 510(k) clearance on 1977-08-04, under 510(k) number K771138.

Who is the listed applicant for PIPETS BOROSILICATE GLASS?

The FDA 510(k) record lists Dade, Baxter Travenol Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PIPETS BOROSILICATE GLASS?

The FDA product code for PIPETS BOROSILICATE GLASS is GJW.

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Related Devices (Code: GJW)

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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.