FDA 510(k)

UMBRELLA KEEL

K-Number: K841348 · 1984-05-02

ApplicantE. Benson Hood Laboratories, Inc.

Decision Date1984-05-02

Product Code

DecisionSubstantially Equivalent

Device Summary

UMBRELLA KEEL is the device name listed in this FDA 510(k) record. The listed applicant is E. Benson Hood Laboratories, Inc.. It received FDA 510(k) clearance on 1984-05-02 under 510(k) number K841348. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UMBRELLA KEEL?

UMBRELLA KEEL is a medical device that received FDA 510(k) clearance on 1984-05-02. The listed applicant is E. Benson Hood Laboratories, Inc.. The 510(k) number is K841348.

When did UMBRELLA KEEL receive FDA 510(k) clearance?

UMBRELLA KEEL received FDA 510(k) clearance on 1984-05-02, under 510(k) number K841348.

Who is the listed applicant for UMBRELLA KEEL?

The FDA 510(k) record lists E. Benson Hood Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing E. Benson Hood Laboratories, Inc. as applicant

K983878CZAJA-MCCAFFREY RIGID STENT INTRODUCER/ENDOSCOPE K841350SALIVARY BYPASS TUBE K841349ESOPHAGEAL TUBE K841266MONTGOMERY TRACHEAL T-TUBE K841347LARYNGEAL STENT

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.