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FDA 510(k)

PICC LINE KIT

K-Number: K952256 · 1995-07-31

ApplicantMedi-Flex Hospital Products, Inc.
Decision Date1995-07-31
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PICC LINE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Flex Hospital Products, Inc.. It received FDA 510(k) clearance on 1995-07-31 under 510(k) number K952256. 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 PICC LINE KIT?

PICC LINE KIT is a medical device that received FDA 510(k) clearance on 1995-07-31. The listed applicant is Medi-Flex Hospital Products, Inc.. The 510(k) number is K952256.

When did PICC LINE KIT receive FDA 510(k) clearance?

PICC LINE KIT received FDA 510(k) clearance on 1995-07-31, under 510(k) number K952256.

Who is the listed applicant for PICC LINE KIT?

The FDA 510(k) record lists Medi-Flex Hospital Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PICC LINE KIT?

The FDA product code for PICC LINE KIT 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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