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FDA 510(k)

STERILE CLOSED SYSTEM

K-Number: K780676 · 1978-05-09

ApplicantMedline Industries, Inc.
Decision Date1978-05-09
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

STERILE CLOSED SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1978-05-09 under 510(k) number K780676. The device is classified under product code KOD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE CLOSED SYSTEM?

STERILE CLOSED SYSTEM is a medical device that received FDA 510(k) clearance on 1978-05-09. The listed applicant is Medline Industries, Inc.. The 510(k) number is K780676.

When did STERILE CLOSED SYSTEM receive FDA 510(k) clearance?

STERILE CLOSED SYSTEM received FDA 510(k) clearance on 1978-05-09, under 510(k) number K780676.

Who is the listed applicant for STERILE CLOSED SYSTEM?

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

What is the FDA product code for STERILE CLOSED SYSTEM?

The FDA product code for STERILE CLOSED SYSTEM is KOD.

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Related Devices (Code: KOD)

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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.

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