FDA 510(k)

ENDO-SPOR PLUS / HYPROCIDE

K-Number: K972708 · 1999-09-13

Decision Date1999-09-13

Product CodeMED

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

ENDO-SPOR PLUS / HYPROCIDE is the device name listed in this FDA 510(k) record. The listed applicant is Cottrell, Ltd.. It received FDA 510(k) clearance on 1999-09-13 under 510(k) number K972708. The device is classified under product code MED. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDO-SPOR PLUS / HYPROCIDE?

ENDO-SPOR PLUS / HYPROCIDE is a medical device that received FDA 510(k) clearance on 1999-09-13. The listed applicant is Cottrell, Ltd.. The 510(k) number is K972708.

When did ENDO-SPOR PLUS / HYPROCIDE receive FDA 510(k) clearance?

ENDO-SPOR PLUS / HYPROCIDE received FDA 510(k) clearance on 1999-09-13, under 510(k) number K972708.

Who is the listed applicant for ENDO-SPOR PLUS / HYPROCIDE?

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

What is the FDA product code for ENDO-SPOR PLUS / HYPROCIDE?

The FDA product code for ENDO-SPOR PLUS / HYPROCIDE is MED.

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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.