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FDA 510(k)

STERILE CORMED MEDIPORT

K-Number: K850967 · 1985-05-17

ApplicantCormed, Inc., Sub. C.R.Bard, Inc.
Decision Date1985-05-17
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILE CORMED MEDIPORT is the device name listed in this FDA 510(k) record. The listed applicant is Cormed, Inc., Sub. C.R.Bard, Inc.. It received FDA 510(k) clearance on 1985-05-17 under 510(k) number K850967. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE CORMED MEDIPORT?

STERILE CORMED MEDIPORT is a medical device that received FDA 510(k) clearance on 1985-05-17. The listed applicant is Cormed, Inc., Sub. C.R.Bard, Inc.. The 510(k) number is K850967.

When did STERILE CORMED MEDIPORT receive FDA 510(k) clearance?

STERILE CORMED MEDIPORT received FDA 510(k) clearance on 1985-05-17, under 510(k) number K850967.

Who is the listed applicant for STERILE CORMED MEDIPORT?

The FDA 510(k) record lists Cormed, Inc., Sub. C.R.Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILE CORMED MEDIPORT?

The FDA product code for STERILE CORMED MEDIPORT is LJT.

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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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