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FDA 510(k)

BI-O.K. EO GAS BIOLOGICAL TEST-PAK (269305,269310,269320)

K-Number: K972747 · 1998-01-09

ApplicantPropper Mfg. Co., Inc.
Decision Date1998-01-09
Product CodeFRC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BI-O.K. EO GAS BIOLOGICAL TEST-PAK (269305,269310,269320) is the device name listed in this FDA 510(k) record. The listed applicant is Propper Mfg. Co., Inc.. It received FDA 510(k) clearance on 1998-01-09 under 510(k) number K972747. 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 BI-O.K. EO GAS BIOLOGICAL TEST-PAK (269305,269310,269320)?

BI-O.K. EO GAS BIOLOGICAL TEST-PAK (269305,269310,269320) is a medical device that received FDA 510(k) clearance on 1998-01-09. The listed applicant is Propper Mfg. Co., Inc.. The 510(k) number is K972747.

When did BI-O.K. EO GAS BIOLOGICAL TEST-PAK (269305,269310,269320) receive FDA 510(k) clearance?

BI-O.K. EO GAS BIOLOGICAL TEST-PAK (269305,269310,269320) received FDA 510(k) clearance on 1998-01-09, under 510(k) number K972747.

Who is the listed applicant for BI-O.K. EO GAS BIOLOGICAL TEST-PAK (269305,269310,269320)?

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

What is the FDA product code for BI-O.K. EO GAS BIOLOGICAL TEST-PAK (269305,269310,269320)?

The FDA product code for BI-O.K. EO GAS BIOLOGICAL TEST-PAK (269305,269310,269320) is FRC.

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Other records listing Propper Mfg. Co., 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.

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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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