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FDA 510(k)

GLOBE RES-Q-FLO

K-Number: K834128 · 1983-12-29

ApplicantGlobe Safety Equipment, Inc.
Decision Date1983-12-29
Product Code
DecisionSubstantially Equivalent

Device Summary

GLOBE RES-Q-FLO is the device name listed in this FDA 510(k) record. The listed applicant is Globe Safety Equipment, Inc.. It received FDA 510(k) clearance on 1983-12-29 under 510(k) number K834128. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLOBE RES-Q-FLO?

GLOBE RES-Q-FLO is a medical device that received FDA 510(k) clearance on 1983-12-29. The listed applicant is Globe Safety Equipment, Inc.. The 510(k) number is K834128.

When did GLOBE RES-Q-FLO receive FDA 510(k) clearance?

GLOBE RES-Q-FLO received FDA 510(k) clearance on 1983-12-29, under 510(k) number K834128.

Who is the listed applicant for GLOBE RES-Q-FLO?

The FDA 510(k) record lists Globe Safety Equipment, Inc. as the applicant. This does not by itself establish the device manufacturer.

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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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Official Source

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