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FDA 510(k)

INTRACATH INTRAVENOUS CATHETER PLACEMENT UNIT

K-Number: K861725 · 1986-12-04

ApplicantParke-Davis Co.
Decision Date1986-12-04
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTRACATH INTRAVENOUS CATHETER PLACEMENT UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Parke-Davis Co.. It received FDA 510(k) clearance on 1986-12-04 under 510(k) number K861725. 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 INTRACATH INTRAVENOUS CATHETER PLACEMENT UNIT?

INTRACATH INTRAVENOUS CATHETER PLACEMENT UNIT is a medical device that received FDA 510(k) clearance on 1986-12-04. The listed applicant is Parke-Davis Co.. The 510(k) number is K861725.

When did INTRACATH INTRAVENOUS CATHETER PLACEMENT UNIT receive FDA 510(k) clearance?

INTRACATH INTRAVENOUS CATHETER PLACEMENT UNIT received FDA 510(k) clearance on 1986-12-04, under 510(k) number K861725.

Who is the listed applicant for INTRACATH INTRAVENOUS CATHETER PLACEMENT UNIT?

The FDA 510(k) record lists Parke-Davis Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTRACATH INTRAVENOUS CATHETER PLACEMENT UNIT?

The FDA product code for INTRACATH INTRAVENOUS CATHETER PLACEMENT UNIT is FOZ.

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Other records listing Parke-Davis Co. as applicant

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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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