FDA 510(k)

LIFESHIELD BLOOD COLLECTION DEVICE

K-Number: K933751 · 1994-02-14

Decision Date1994-02-14

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

LIFESHIELD BLOOD COLLECTION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1994-02-14 under 510(k) number K933751. 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 LIFESHIELD BLOOD COLLECTION DEVICE?

LIFESHIELD BLOOD COLLECTION DEVICE is a medical device that received FDA 510(k) clearance on 1994-02-14. The listed applicant is Sherwood Medical Co.. The 510(k) number is K933751.

When did LIFESHIELD BLOOD COLLECTION DEVICE receive FDA 510(k) clearance?

LIFESHIELD BLOOD COLLECTION DEVICE received FDA 510(k) clearance on 1994-02-14, under 510(k) number K933751.

Who is the listed applicant for LIFESHIELD BLOOD COLLECTION DEVICE?

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

What is the FDA product code for LIFESHIELD BLOOD COLLECTION DEVICE?

The FDA product code for LIFESHIELD BLOOD COLLECTION DEVICE is 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.