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FDA 510(k)

MODIFICATION TO RAVEN BACTERIAL SPORE STRIPS

K-Number: K050591 · 2005-03-23

ApplicantRaven Biological Laboratories, Inc.
Decision Date2005-03-23
Product CodeFRC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO RAVEN BACTERIAL SPORE STRIPS 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 2005-03-23 under 510(k) number K050591. 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 MODIFICATION TO RAVEN BACTERIAL SPORE STRIPS?

MODIFICATION TO RAVEN BACTERIAL SPORE STRIPS is a medical device that received FDA 510(k) clearance on 2005-03-23. The listed applicant is Raven Biological Laboratories, Inc.. The 510(k) number is K050591.

When did MODIFICATION TO RAVEN BACTERIAL SPORE STRIPS receive FDA 510(k) clearance?

MODIFICATION TO RAVEN BACTERIAL SPORE STRIPS received FDA 510(k) clearance on 2005-03-23, under 510(k) number K050591.

Who is the listed applicant for MODIFICATION TO RAVEN BACTERIAL SPORE STRIPS?

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 MODIFICATION TO RAVEN BACTERIAL SPORE STRIPS?

The FDA product code for MODIFICATION TO RAVEN BACTERIAL SPORE STRIPS 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 PROPACTK041784RAVEN PROTEST - EOK041386RAVEN PROTEST - STEAMK032914MODIFICATION TO:RAVEN BACTERIAL SPORE STRIPS

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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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