FDA 510(k)

BUTTERFLY NON-CORING NEEDLE SET

K-Number: K863606 · 1986-12-18

ApplicantCormed, Inc., Sub. C.R.Bard, Inc.

Decision Date1986-12-18

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

BUTTERFLY NON-CORING NEEDLE SET 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 1986-12-18 under 510(k) number K863606. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BUTTERFLY NON-CORING NEEDLE SET?

BUTTERFLY NON-CORING NEEDLE SET is a medical device that received FDA 510(k) clearance on 1986-12-18. The listed applicant is Cormed, Inc., Sub. C.R.Bard, Inc.. The 510(k) number is K863606.

When did BUTTERFLY NON-CORING NEEDLE SET receive FDA 510(k) clearance?

BUTTERFLY NON-CORING NEEDLE SET received FDA 510(k) clearance on 1986-12-18, under 510(k) number K863606.

Who is the listed applicant for BUTTERFLY NON-CORING NEEDLE SET?

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 BUTTERFLY NON-CORING NEEDLE SET?

The FDA product code for BUTTERFLY NON-CORING NEEDLE SET is FMI.

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Related Devices (Code: FMI)

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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.