FDA 510(k)

PERIMETER SUMP DRAIN

K-Number: K844923 · 1985-03-18

Decision Date1985-03-18

Product Code

DecisionSubstantially Equivalent

Device Summary

PERIMETER SUMP DRAIN is the device name listed in this FDA 510(k) record. The listed applicant is Perimeter Medical, Inc.. It received FDA 510(k) clearance on 1985-03-18 under 510(k) number K844923. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIMETER SUMP DRAIN?

PERIMETER SUMP DRAIN is a medical device that received FDA 510(k) clearance on 1985-03-18. The listed applicant is Perimeter Medical, Inc.. The 510(k) number is K844923.

When did PERIMETER SUMP DRAIN receive FDA 510(k) clearance?

PERIMETER SUMP DRAIN received FDA 510(k) clearance on 1985-03-18, under 510(k) number K844923.

Who is the listed applicant for PERIMETER SUMP DRAIN?

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

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Other records listing Perimeter Medical, Inc. as applicant

K844921PERIMETER CLOSED WOUND RESEVOIR K844924PERIMETER YANKAUER SUCTION TIPS & SETS K844925PERIMETER MEDIASTINAL DRAIN K844922PERIMETER THORACIC CATHETER

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.