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)

PROBE PERSONAL PREFERENCE NON-STER. PAT. EXAM.GLOV

K-Number: K930903 · 1993-08-25

Decision Date1993-08-25
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PROBE PERSONAL PREFERENCE NON-STER. PAT. EXAM.GLOV is the device name listed in this FDA 510(k) record. The listed applicant is Glove India Private , Ltd.. It received FDA 510(k) clearance on 1993-08-25 under 510(k) number K930903. 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 PROBE PERSONAL PREFERENCE NON-STER. PAT. EXAM.GLOV?

PROBE PERSONAL PREFERENCE NON-STER. PAT. EXAM.GLOV is a medical device that received FDA 510(k) clearance on 1993-08-25. The listed applicant is Glove India Private , Ltd.. The 510(k) number is K930903.

When did PROBE PERSONAL PREFERENCE NON-STER. PAT. EXAM.GLOV receive FDA 510(k) clearance?

PROBE PERSONAL PREFERENCE NON-STER. PAT. EXAM.GLOV received FDA 510(k) clearance on 1993-08-25, under 510(k) number K930903.

Who is the listed applicant for PROBE PERSONAL PREFERENCE NON-STER. PAT. EXAM.GLOV?

The FDA 510(k) record lists Glove India Private , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROBE PERSONAL PREFERENCE NON-STER. PAT. EXAM.GLOV?

The FDA product code for PROBE PERSONAL PREFERENCE NON-STER. PAT. EXAM.GLOV 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 Glove India Private , 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.

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.

↑