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FDA 510(k), K014087, LATEXX MANUFACTURING NON-CHLORINATED, POLYMER COATED, POWDER-FREE RUBBER LATEX EXAMINATION GLOVE
FDA 510(k), K014087, LATEXX MANUFACTURING NON-CHLORINATED, POLYMER COATED, POWDER-FREE RUBBER LATEX EXAMINATION GLOVE
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510(K) Number: K014087
Device Name: LATEXX MANUFACTURING NON-CHLORINATED, POLYMER COATED, POWDER-FREE RUBBER LATEX EXAMINATION GLOVE
Manufacturer: LATEXX MANUFACTURING SDN.BHD.
Device Classification Name: latex patient examination glove
Regulation Number: 880.6250
Classification Product Code: LYY
Date Received: 12/11/2001
Decision Date: 03/04/2002
Regulation Medical Specialty: General Hospital
Device Name: LATEXX MANUFACTURING NON-CHLORINATED, POLYMER COATED, POWDER-FREE RUBBER LATEX EXAMINATION GLOVE
Manufacturer: LATEXX MANUFACTURING SDN.BHD.
Device Classification Name: latex patient examination glove
Regulation Number: 880.6250
Classification Product Code: LYY
Date Received: 12/11/2001
Decision Date: 03/04/2002
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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