SMARTTEX PREPOWDERED LATEX EXAMINATION GLOVES
K-Number: K981348 · 1998-05-18
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Device Summary
Frequently Asked Questions
What is the SMARTTEX PREPOWDERED LATEX EXAMINATION GLOVES?
SMARTTEX PREPOWDERED LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1998-05-18. The listed applicant is Smart Glove Corp. Sdn Bhd. The 510(k) number is K981348.
When did SMARTTEX PREPOWDERED LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?
SMARTTEX PREPOWDERED LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1998-05-18, under 510(k) number K981348.
Who is the listed applicant for SMARTTEX PREPOWDERED LATEX EXAMINATION GLOVES?
The FDA 510(k) record lists Smart Glove Corp. Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SMARTTEX PREPOWDERED LATEX EXAMINATION GLOVES?
The FDA product code for SMARTTEX PREPOWDERED LATEX EXAMINATION GLOVES 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 Smart Glove Corp. Sdn Bhd 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.
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