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FDA 510(k)

CYPRESS MEDICAL PRODUCTS STERILE LATEX EXAMINATION GLOVE

K-Number: K950254 · 1995-03-31

Decision Date1995-03-31
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CYPRESS MEDICAL PRODUCTS STERILE LATEX EXAMINATION GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Cypress Medical Products, Ltd.. It received FDA 510(k) clearance on 1995-03-31 under 510(k) number K950254. 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 CYPRESS MEDICAL PRODUCTS STERILE LATEX EXAMINATION GLOVE?

CYPRESS MEDICAL PRODUCTS STERILE LATEX EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1995-03-31. The listed applicant is Cypress Medical Products, Ltd.. The 510(k) number is K950254.

When did CYPRESS MEDICAL PRODUCTS STERILE LATEX EXAMINATION GLOVE receive FDA 510(k) clearance?

CYPRESS MEDICAL PRODUCTS STERILE LATEX EXAMINATION GLOVE received FDA 510(k) clearance on 1995-03-31, under 510(k) number K950254.

Who is the listed applicant for CYPRESS MEDICAL PRODUCTS STERILE LATEX EXAMINATION GLOVE?

The FDA 510(k) record lists Cypress Medical Products, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CYPRESS MEDICAL PRODUCTS STERILE LATEX EXAMINATION GLOVE?

The FDA product code for CYPRESS MEDICAL PRODUCTS STERILE LATEX EXAMINATION GLOVE 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 Cypress Medical Products, Ltd. 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 26 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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