PROBE PERSONAL PREFERENCE NON-STER. PAT. EXAM.GLOV
K-Number: K930903 · 1993-08-25
Advertisement
Device Summary
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.
Advertisement