FDA 510(k)

K-MED SILICONE SUMP DRAIN

K-Number: K812026 · 1981-08-31

Decision Date1981-08-31

Product Code

DecisionSubstantially Equivalent

Device Summary

K-MED SILICONE SUMP DRAIN is the device name listed in this FDA 510(k) record. The listed applicant is K-Med, Inc.. It received FDA 510(k) clearance on 1981-08-31 under 510(k) number K812026. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the K-MED SILICONE SUMP DRAIN?

K-MED SILICONE SUMP DRAIN is a medical device that received FDA 510(k) clearance on 1981-08-31. The listed applicant is K-Med, Inc.. The 510(k) number is K812026.

When did K-MED SILICONE SUMP DRAIN receive FDA 510(k) clearance?

K-MED SILICONE SUMP DRAIN received FDA 510(k) clearance on 1981-08-31, under 510(k) number K812026.

Who is the listed applicant for K-MED SILICONE SUMP DRAIN?

The FDA 510(k) record lists K-Med, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing K-Med, Inc. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.