SENSIFLEX POWDERFREE SURGEON'S GLOVE
K-Number: K982957 · 1999-01-13
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Device Summary
Frequently Asked Questions
What is the SENSIFLEX POWDERFREE SURGEON'S GLOVE?
SENSIFLEX POWDERFREE SURGEON'S GLOVE is a medical device that received FDA 510(k) clearance on 1999-01-13. The listed applicant is Terang Nusa Sdn Bhd. The 510(k) number is K982957.
When did SENSIFLEX POWDERFREE SURGEON'S GLOVE receive FDA 510(k) clearance?
SENSIFLEX POWDERFREE SURGEON'S GLOVE received FDA 510(k) clearance on 1999-01-13, under 510(k) number K982957.
Who is the listed applicant for SENSIFLEX POWDERFREE SURGEON'S GLOVE?
The FDA 510(k) record lists Terang Nusa Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SENSIFLEX POWDERFREE SURGEON'S GLOVE?
The FDA product code for SENSIFLEX POWDERFREE SURGEON'S GLOVE is KGO.
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 Terang Nusa 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: KGO)
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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