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FDA 510(k)

CORMED II AMBULATORY INFUSION PUMP

K-Number: K850674 · 1985-04-09

ApplicantCormed, Inc., Sub. C.R.Bard, Inc.
Decision Date1985-04-09
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CORMED II AMBULATORY INFUSION PUMP 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 1985-04-09 under 510(k) number K850674. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORMED II AMBULATORY INFUSION PUMP?

CORMED II AMBULATORY INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1985-04-09. The listed applicant is Cormed, Inc., Sub. C.R.Bard, Inc.. The 510(k) number is K850674.

When did CORMED II AMBULATORY INFUSION PUMP receive FDA 510(k) clearance?

CORMED II AMBULATORY INFUSION PUMP received FDA 510(k) clearance on 1985-04-09, under 510(k) number K850674.

Who is the listed applicant for CORMED II AMBULATORY INFUSION PUMP?

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 CORMED II AMBULATORY INFUSION PUMP?

The FDA product code for CORMED II AMBULATORY INFUSION PUMP is FRN.

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Related Devices (Code: FRN)

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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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