FDA 510(k)

PENROSE DRAINS

K-Number: K841037 · 1984-04-25

Decision Date1984-04-25

Product Code

DecisionSubstantially Equivalent

Device Summary

PENROSE DRAINS is the device name listed in this FDA 510(k) record. The listed applicant is Inmed Corp.. It received FDA 510(k) clearance on 1984-04-25 under 510(k) number K841037. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PENROSE DRAINS?

PENROSE DRAINS is a medical device that received FDA 510(k) clearance on 1984-04-25. The listed applicant is Inmed Corp.. The 510(k) number is K841037.

When did PENROSE DRAINS receive FDA 510(k) clearance?

PENROSE DRAINS received FDA 510(k) clearance on 1984-04-25, under 510(k) number K841037.

Who is the listed applicant for PENROSE DRAINS?

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

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Other records listing Inmed Corp. 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.