FDA 510(k)

GLOBIN-TERGE

K-Number: K780817 · 1978-07-27

Decision Date1978-07-27

Product Code

DecisionSubstantially Equivalent

Device Summary

GLOBIN-TERGE is the device name listed in this FDA 510(k) record. The listed applicant is Simmler & Son, Inc.. It received FDA 510(k) clearance on 1978-07-27 under 510(k) number K780817. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLOBIN-TERGE?

GLOBIN-TERGE is a medical device that received FDA 510(k) clearance on 1978-07-27. The listed applicant is Simmler & Son, Inc.. The 510(k) number is K780817.

When did GLOBIN-TERGE receive FDA 510(k) clearance?

GLOBIN-TERGE received FDA 510(k) clearance on 1978-07-27, under 510(k) number K780817.

Who is the listed applicant for GLOBIN-TERGE?

The FDA 510(k) record lists Simmler & Son, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Simmler & Son, Inc. as applicant

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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.