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FDA 510(k)

CATHETER-THRU-NEEDLE DEVICE

K-Number: K770403 · 1977-03-16

ApplicantAbbott Laboratories
Decision Date1977-03-16
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CATHETER-THRU-NEEDLE DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1977-03-16 under 510(k) number K770403. 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 CATHETER-THRU-NEEDLE DEVICE?

CATHETER-THRU-NEEDLE DEVICE is a medical device that received FDA 510(k) clearance on 1977-03-16. The listed applicant is Abbott Laboratories. The 510(k) number is K770403.

When did CATHETER-THRU-NEEDLE DEVICE receive FDA 510(k) clearance?

CATHETER-THRU-NEEDLE DEVICE received FDA 510(k) clearance on 1977-03-16, under 510(k) number K770403.

Who is the listed applicant for CATHETER-THRU-NEEDLE DEVICE?

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 CATHETER-THRU-NEEDLE DEVICE?

The FDA product code for CATHETER-THRU-NEEDLE DEVICE is FOZ.

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Related Devices (Code: 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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