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FDA 510(k)

FAST'N'FLAMMATORY KIT

K-Number: K931241 · 1994-02-03

ApplicantTechlab, Inc.
Decision Date1994-02-03
Product CodeGIA
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

FAST'N'FLAMMATORY KIT is the device name listed in this FDA 510(k) record. The listed applicant is Techlab, Inc.. It received FDA 510(k) clearance on 1994-02-03 under 510(k) number K931241. The device is classified under product code GIA. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FAST'N'FLAMMATORY KIT?

FAST'N'FLAMMATORY KIT is a medical device that received FDA 510(k) clearance on 1994-02-03. The listed applicant is Techlab, Inc.. The 510(k) number is K931241.

When did FAST'N'FLAMMATORY KIT receive FDA 510(k) clearance?

FAST'N'FLAMMATORY KIT received FDA 510(k) clearance on 1994-02-03, under 510(k) number K931241.

Who is the listed applicant for FAST'N'FLAMMATORY KIT?

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

What is the FDA product code for FAST'N'FLAMMATORY KIT?

The FDA product code for FAST'N'FLAMMATORY KIT is GIA.

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Related Devices (Code: GIA)

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

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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