510(k) K914157
K914157 is an FDA 510(k) premarket notification submitted by Cml, Inc. for the device "DRESSING/CVP DRESSING CHANGE/HYPERALIMENT TRAYS". The FDA issued a decision of Substantially Equivalent (kit, denovo) on December 13, 1991. The device falls under product code LYY (Latex Patient Examination Glove), a Class I device regulated under 21 CFR 880.6250. Cml, Inc. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SEKD (Substantially Equivalent (kit, denovo))
- Decision Date
- December 13, 1991
- Date Received
- September 16, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Latex Patient Examination Glove
- Device Class
- Class I
- Regulation Number
- 880.6250
- Review Panel
- HO
- Submission Type
A latex patient examination glove is a disposable device made of natural rubber latex that may or may not bear a trace amount of residual powder, and is intended to be worn on the hand for medical purposes to provide a barrier against potentially infectious materials and other contaminants.