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FDA 510(k)

NEEDLE CONNECTING SET, BLUNT

K-Number: K780105 · 1978-02-21

ApplicantAbbott Laboratories
Decision Date1978-02-21
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NEEDLE CONNECTING SET, BLUNT is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1978-02-21 under 510(k) number K780105. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEEDLE CONNECTING SET, BLUNT?

NEEDLE CONNECTING SET, BLUNT is a medical device that received FDA 510(k) clearance on 1978-02-21. The listed applicant is Abbott Laboratories. The 510(k) number is K780105.

When did NEEDLE CONNECTING SET, BLUNT receive FDA 510(k) clearance?

NEEDLE CONNECTING SET, BLUNT received FDA 510(k) clearance on 1978-02-21, under 510(k) number K780105.

Who is the listed applicant for NEEDLE CONNECTING SET, BLUNT?

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

What is the FDA product code for NEEDLE CONNECTING SET, BLUNT?

The FDA product code for NEEDLE CONNECTING SET, BLUNT is FOZ.

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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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