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FDA 510(k), K923862, LATEX PATIENT EXAMINATION GLOVE (POWDER FREE)
FDA 510(k), K923862, LATEX PATIENT EXAMINATION GLOVE (POWDER FREE)
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510(K) Number: K923862
Device Name: LATEX PATIENT EXAMINATION GLOVE (POWDER FREE)
Manufacturer: SIAM SEMPERMED CORP. LTD.
Device Classification Name: latex patient examination glove
Regulation Number: 880.6250
Classification Product Code: LYY
Date Received: 08/03/1992
Decision Date: 02/10/1993
Regulation Medical Specialty: General Hospital
Device Name: LATEX PATIENT EXAMINATION GLOVE (POWDER FREE)
Manufacturer: SIAM SEMPERMED CORP. LTD.
Device Classification Name: latex patient examination glove
Regulation Number: 880.6250
Classification Product Code: LYY
Date Received: 08/03/1992
Decision Date: 02/10/1993
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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