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FDA 510(k)

BIOSHIELD BLUE LATEX GLOVES

K-Number: K940256 · 1994-03-23

Decision Date1994-03-23
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BIOSHIELD BLUE LATEX GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Chester Labs, Inc.. It received FDA 510(k) clearance on 1994-03-23 under 510(k) number K940256. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOSHIELD BLUE LATEX GLOVES?

BIOSHIELD BLUE LATEX GLOVES is a medical device that received FDA 510(k) clearance on 1994-03-23. The listed applicant is Chester Labs, Inc.. The 510(k) number is K940256.

When did BIOSHIELD BLUE LATEX GLOVES receive FDA 510(k) clearance?

BIOSHIELD BLUE LATEX GLOVES received FDA 510(k) clearance on 1994-03-23, under 510(k) number K940256.

Who is the listed applicant for BIOSHIELD BLUE LATEX GLOVES?

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

What is the FDA product code for BIOSHIELD BLUE LATEX GLOVES?

The FDA product code for BIOSHIELD BLUE LATEX GLOVES is LYY.

Related Clinical Trials

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.

Other records listing Chester Labs, 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.

View all 11 devices →

Related Devices (Code: LYY)

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.

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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