FDA 510(k)

SPORDEX CULTURE MEDIA

K-Number: K850143 · 1985-03-05

Decision Date1985-03-05

Product CodeJSC

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

SPORDEX CULTURE MEDIA is the device name listed in this FDA 510(k) record. The listed applicant is American Sterilizer Co.. It received FDA 510(k) clearance on 1985-03-05 under 510(k) number K850143. The device is classified under product code JSC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPORDEX CULTURE MEDIA?

SPORDEX CULTURE MEDIA is a medical device that received FDA 510(k) clearance on 1985-03-05. The listed applicant is American Sterilizer Co.. The 510(k) number is K850143.

When did SPORDEX CULTURE MEDIA receive FDA 510(k) clearance?

SPORDEX CULTURE MEDIA received FDA 510(k) clearance on 1985-03-05, under 510(k) number K850143.

Who is the listed applicant for SPORDEX CULTURE MEDIA?

The FDA 510(k) record lists American Sterilizer Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPORDEX CULTURE MEDIA?

The FDA product code for SPORDEX CULTURE MEDIA is JSC.

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Other records listing American Sterilizer Co. as applicant

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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.