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FDA 510(k)

MODIFIED PATIENT EXAMINATION GLOVES

K-Number: K894311 · 1989-08-10

Decision Date1989-08-10
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODIFIED PATIENT EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Safeskin Corp.. It received FDA 510(k) clearance on 1989-08-10 under 510(k) number K894311. 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 MODIFIED PATIENT EXAMINATION GLOVES?

MODIFIED PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-08-10. The listed applicant is Safeskin Corp.. The 510(k) number is K894311.

When did MODIFIED PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?

MODIFIED PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 1989-08-10, under 510(k) number K894311.

Who is the listed applicant for MODIFIED PATIENT EXAMINATION GLOVES?

The FDA 510(k) record lists Safeskin Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED PATIENT EXAMINATION GLOVES?

The FDA product code for MODIFIED PATIENT EXAMINATION 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 Safeskin Corp. 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 24 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

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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