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FDA 510(k)

BETHEL PLUS MULTIPLE NAMES

K-Number: K912042 · 1991-07-02

ApplicantBethel Latex Products, Inc.
Decision Date1991-07-02
Product CodeLZB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BETHEL PLUS MULTIPLE NAMES is the device name listed in this FDA 510(k) record. The listed applicant is Bethel Latex Products, Inc.. It received FDA 510(k) clearance on 1991-07-02 under 510(k) number K912042. The device is classified under product code LZB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BETHEL PLUS MULTIPLE NAMES?

BETHEL PLUS MULTIPLE NAMES is a medical device that received FDA 510(k) clearance on 1991-07-02. The listed applicant is Bethel Latex Products, Inc.. The 510(k) number is K912042.

When did BETHEL PLUS MULTIPLE NAMES receive FDA 510(k) clearance?

BETHEL PLUS MULTIPLE NAMES received FDA 510(k) clearance on 1991-07-02, under 510(k) number K912042.

Who is the listed applicant for BETHEL PLUS MULTIPLE NAMES?

The FDA 510(k) record lists Bethel Latex Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BETHEL PLUS MULTIPLE NAMES?

The FDA product code for BETHEL PLUS MULTIPLE NAMES is LZB.

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Related Devices (Code: LZB)

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.

K052387ARTHREX FINGERSHIELD FINGER GUARD, MODEL AR-7199-XXArthrex, Inc.K992539PERCUGUARDDigit-ProK980827LATEX FINGER COT, POWDER-FREE, WITH PROTEIN LABELINGTucker & AssociatesK903073LATEX FINGER COTSDongkuk Trading Co., Ltd.

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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