FDA 510(k)

FLASH GUARD

K-Number: K841669 · 1984-06-05

Decision Date1984-06-05

Product Code

DecisionSubstantially Equivalent

Device Summary

FLASH GUARD is the device name listed in this FDA 510(k) record. The listed applicant is Sparco, Inc.. It received FDA 510(k) clearance on 1984-06-05 under 510(k) number K841669. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLASH GUARD?

FLASH GUARD is a medical device that received FDA 510(k) clearance on 1984-06-05. The listed applicant is Sparco, Inc.. The 510(k) number is K841669.

When did FLASH GUARD receive FDA 510(k) clearance?

FLASH GUARD received FDA 510(k) clearance on 1984-06-05, under 510(k) number K841669.

Who is the listed applicant for FLASH GUARD?

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

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Sparco, Inc. as applicant

K884041MASTER-GUARD K863964LIMB-GUARD K850268SPARCO SCOPE GUARD K850267SPARCO PIGGY-BACK POLE-INTRAVENOUS TRANSPORT POLE K844286FLASH GUARD PLASTIC VERSION

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.