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FDA 510(k)

SALIVARY BYPASS TUBE

K-Number: K841350 · 1984-07-26

ApplicantE. Benson Hood Laboratories, Inc.
Decision Date1984-07-26
Product Code
DecisionSubstantially Equivalent

Device Summary

SALIVARY BYPASS TUBE 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 1984-07-26 under 510(k) number K841350. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SALIVARY BYPASS TUBE?

SALIVARY BYPASS TUBE is a medical device that received FDA 510(k) clearance on 1984-07-26. The listed applicant is E. Benson Hood Laboratories, Inc.. The 510(k) number is K841350.

When did SALIVARY BYPASS TUBE receive FDA 510(k) clearance?

SALIVARY BYPASS TUBE received FDA 510(k) clearance on 1984-07-26, under 510(k) number K841350.

Who is the listed applicant for SALIVARY BYPASS TUBE?

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

Related Clinical Trials

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

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.

K983878CZAJA-MCCAFFREY RIGID STENT INTRODUCER/ENDOSCOPEK841349ESOPHAGEAL TUBEK841266MONTGOMERY TRACHEAL T-TUBEK841348UMBRELLA KEELK841347LARYNGEAL STENT

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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