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FDA 510(k)

LIFESHIELD BLUNT CANNULA

K-Number: K963351 · 1997-02-26

ApplicantAbbott Laboratories
Decision Date1997-02-26
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIFESHIELD BLUNT CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1997-02-26 under 510(k) number K963351. 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 BLUNT CANNULA?

LIFESHIELD BLUNT CANNULA is a medical device that received FDA 510(k) clearance on 1997-02-26. The listed applicant is Abbott Laboratories. The 510(k) number is K963351.

When did LIFESHIELD BLUNT CANNULA receive FDA 510(k) clearance?

LIFESHIELD BLUNT CANNULA received FDA 510(k) clearance on 1997-02-26, under 510(k) number K963351.

Who is the listed applicant for LIFESHIELD BLUNT CANNULA?

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 LIFESHIELD BLUNT CANNULA?

The FDA product code for LIFESHIELD BLUNT CANNULA is FMI.

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Related Devices (Code: FMI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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