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FDA 510(k)

PTI - LATEX EXAMINATION GLOVES

K-Number: K890456 · 1989-03-23

ApplicantPrecision Trading Intl., Inc.
Decision Date1989-03-23
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PTI - LATEX EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Precision Trading Intl., Inc.. It received FDA 510(k) clearance on 1989-03-23 under 510(k) number K890456. 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 PTI - LATEX EXAMINATION GLOVES?

PTI - LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-03-23. The listed applicant is Precision Trading Intl., Inc.. The 510(k) number is K890456.

When did PTI - LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?

PTI - LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1989-03-23, under 510(k) number K890456.

Who is the listed applicant for PTI - LATEX EXAMINATION GLOVES?

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

What is the FDA product code for PTI - LATEX EXAMINATION GLOVES?

The FDA product code for PTI - LATEX EXAMINATION GLOVES is LYY.

Related Clinical Trials

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Other records listing Precision Trading Intl., 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.

K891934ADDWEALTH LATEX EXAMINATION GLOVES

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.

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Official Source

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