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FDA 510(k)

ABELSON CRICOTHYROTOMY CANNULA

K-Number: K952401 · 1995-07-11

ApplicantGilbert Surgical Instruments, Inc.
Decision Date1995-07-11
Product CodeBWC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ABELSON CRICOTHYROTOMY CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Gilbert Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1995-07-11 under 510(k) number K952401. The device is classified under product code BWC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABELSON CRICOTHYROTOMY CANNULA?

ABELSON CRICOTHYROTOMY CANNULA is a medical device that received FDA 510(k) clearance on 1995-07-11. The listed applicant is Gilbert Surgical Instruments, Inc.. The 510(k) number is K952401.

When did ABELSON CRICOTHYROTOMY CANNULA receive FDA 510(k) clearance?

ABELSON CRICOTHYROTOMY CANNULA received FDA 510(k) clearance on 1995-07-11, under 510(k) number K952401.

Who is the listed applicant for ABELSON CRICOTHYROTOMY CANNULA?

The FDA 510(k) record lists Gilbert Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ABELSON CRICOTHYROTOMY CANNULA?

The FDA product code for ABELSON CRICOTHYROTOMY CANNULA is BWC.

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Related Devices (Code: BWC)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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