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FDA 510(k)

POWDERFREE POLYCHLOROPRENE STERILIZED SURGICAL GLOVES

K-Number: K030228 · 2003-03-14

Decision Date2003-03-14
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

POWDERFREE POLYCHLOROPRENE STERILIZED SURGICAL GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Pt. Medisafe Technologies. It received FDA 510(k) clearance on 2003-03-14 under 510(k) number K030228. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWDERFREE POLYCHLOROPRENE STERILIZED SURGICAL GLOVES?

POWDERFREE POLYCHLOROPRENE STERILIZED SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 2003-03-14. The listed applicant is Pt. Medisafe Technologies. The 510(k) number is K030228.

When did POWDERFREE POLYCHLOROPRENE STERILIZED SURGICAL GLOVES receive FDA 510(k) clearance?

POWDERFREE POLYCHLOROPRENE STERILIZED SURGICAL GLOVES received FDA 510(k) clearance on 2003-03-14, under 510(k) number K030228.

Who is the listed applicant for POWDERFREE POLYCHLOROPRENE STERILIZED SURGICAL GLOVES?

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

What is the FDA product code for POWDERFREE POLYCHLOROPRENE STERILIZED SURGICAL GLOVES?

The FDA product code for POWDERFREE POLYCHLOROPRENE STERILIZED SURGICAL GLOVES is KGO.

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 Pt. Medisafe Technologies 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 16 devices →

Related Devices (Code: KGO)

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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