Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PATIENT EXAM GLOVES (MFG. WOOD TING INDUSTRY)

K-Number: K892752 · 1989-06-06

Decision Date1989-06-06
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAM GLOVES (MFG. WOOD TING INDUSTRY) is the device name listed in this FDA 510(k) record. The listed applicant is Foodhandler, Inc.. It received FDA 510(k) clearance on 1989-06-06 under 510(k) number K892752. 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 PATIENT EXAM GLOVES (MFG. WOOD TING INDUSTRY)?

PATIENT EXAM GLOVES (MFG. WOOD TING INDUSTRY) is a medical device that received FDA 510(k) clearance on 1989-06-06. The listed applicant is Foodhandler, Inc.. The 510(k) number is K892752.

When did PATIENT EXAM GLOVES (MFG. WOOD TING INDUSTRY) receive FDA 510(k) clearance?

PATIENT EXAM GLOVES (MFG. WOOD TING INDUSTRY) received FDA 510(k) clearance on 1989-06-06, under 510(k) number K892752.

Who is the listed applicant for PATIENT EXAM GLOVES (MFG. WOOD TING INDUSTRY)?

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

What is the FDA product code for PATIENT EXAM GLOVES (MFG. WOOD TING INDUSTRY)?

The FDA product code for PATIENT EXAM GLOVES (MFG. WOOD TING INDUSTRY) 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 Foodhandler, 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.

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.

↑