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FDA 510(k)

SPORE STRIP

K-Number: K912796 · 1992-04-02

ApplicantRaven Biological Laboratories, Inc.
Decision Date1992-04-02
Product CodeFRC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SPORE STRIP is the device name listed in this FDA 510(k) record. The listed applicant is Raven Biological Laboratories, Inc.. It received FDA 510(k) clearance on 1992-04-02 under 510(k) number K912796. The device is classified under product code FRC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPORE STRIP?

SPORE STRIP is a medical device that received FDA 510(k) clearance on 1992-04-02. The listed applicant is Raven Biological Laboratories, Inc.. The 510(k) number is K912796.

When did SPORE STRIP receive FDA 510(k) clearance?

SPORE STRIP received FDA 510(k) clearance on 1992-04-02, under 510(k) number K912796.

Who is the listed applicant for SPORE STRIP?

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

What is the FDA product code for SPORE STRIP?

The FDA product code for SPORE STRIP is FRC.

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Other records listing Raven Biological Laboratories, Inc. as applicant

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.

K082756RAVEN PROTEST - STEAM BIOLOGICAL INDICATORK062651PROCHEM EXT CHEMICAL INTEGRATORK053212RAVEN PROPACTK050591MODIFICATION TO RAVEN BACTERIAL SPORE STRIPSK041784RAVEN PROTEST - EOK041386RAVEN PROTEST - STEAM

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Related Devices (Code: FRC)

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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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