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FDA 510(k)

TELEFLEX MEDICAL INTRODUCER NEEDLE

K-Number: K851140 · 1985-06-19

ApplicantTeleflexmedical, Inc.
Decision Date1985-06-19
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TELEFLEX MEDICAL INTRODUCER NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Teleflexmedical, Inc.. It received FDA 510(k) clearance on 1985-06-19 under 510(k) number K851140. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TELEFLEX MEDICAL INTRODUCER NEEDLE?

TELEFLEX MEDICAL INTRODUCER NEEDLE is a medical device that received FDA 510(k) clearance on 1985-06-19. The listed applicant is Teleflexmedical, Inc.. The 510(k) number is K851140.

When did TELEFLEX MEDICAL INTRODUCER NEEDLE receive FDA 510(k) clearance?

TELEFLEX MEDICAL INTRODUCER NEEDLE received FDA 510(k) clearance on 1985-06-19, under 510(k) number K851140.

Who is the listed applicant for TELEFLEX MEDICAL INTRODUCER NEEDLE?

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

What is the FDA product code for TELEFLEX MEDICAL INTRODUCER NEEDLE?

The FDA product code for TELEFLEX MEDICAL INTRODUCER NEEDLE is DWS.

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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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