FDA 510(k)

PROTECTIV SAFETY BLOOD COLLECTION NEEDLE

K-Number: K001690 · 2000-07-31

ApplicantJohnson & Johnson Medical, Inc.

Decision Date2000-07-31

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PROTECTIV SAFETY BLOOD COLLECTION NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Medical, Inc.. It received FDA 510(k) clearance on 2000-07-31 under 510(k) number K001690. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROTECTIV SAFETY BLOOD COLLECTION NEEDLE?

PROTECTIV SAFETY BLOOD COLLECTION NEEDLE is a medical device that received FDA 510(k) clearance on 2000-07-31. The listed applicant is Johnson & Johnson Medical, Inc.. The 510(k) number is K001690.

When did PROTECTIV SAFETY BLOOD COLLECTION NEEDLE receive FDA 510(k) clearance?

PROTECTIV SAFETY BLOOD COLLECTION NEEDLE received FDA 510(k) clearance on 2000-07-31, under 510(k) number K001690.

Who is the listed applicant for PROTECTIV SAFETY BLOOD COLLECTION NEEDLE?

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

What is the FDA product code for PROTECTIV SAFETY BLOOD COLLECTION NEEDLE?

The FDA product code for PROTECTIV SAFETY BLOOD COLLECTION NEEDLE is FMI.

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Related Devices (Code: FMI)

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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.