FDA 510(k)

CATHETERS, OVER-THE-NEEDLE

K-Number: K770751 · 1977-05-26

Decision Date1977-05-26

Product CodeFOZ

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

CATHETERS, OVER-THE-NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Cutter Laboratories, Inc.. It received FDA 510(k) clearance on 1977-05-26 under 510(k) number K770751. 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 CATHETERS, OVER-THE-NEEDLE?

CATHETERS, OVER-THE-NEEDLE is a medical device that received FDA 510(k) clearance on 1977-05-26. The listed applicant is Cutter Laboratories, Inc.. The 510(k) number is K770751.

When did CATHETERS, OVER-THE-NEEDLE receive FDA 510(k) clearance?

CATHETERS, OVER-THE-NEEDLE received FDA 510(k) clearance on 1977-05-26, under 510(k) number K770751.

Who is the listed applicant for CATHETERS, OVER-THE-NEEDLE?

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

What is the FDA product code for CATHETERS, OVER-THE-NEEDLE?

The FDA product code for CATHETERS, OVER-THE-NEEDLE is FOZ.

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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.