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FDA 510(k) Application Details - K980677
Device Classification Name
Polymer Patient Examination Glove
More FDA Info for this Device
510(K) Number
K980677
Device Name
Polymer Patient Examination Glove
Applicant
NINGBO YUJIANG PLASTIC & RUBBER CO. LTD.
19001 S. RICHFIELD
#185
GREEN VALLEY, AZ 85614 US
Other 510(k) Applications for this Company
Contact
JANNA P TUCKER
Other 510(k) Applications for this Contact
Regulation Number
880.6250
More FDA Info for this Regulation Number
Classification Product Code
LZA
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/20/1998
Decision Date
03/16/1998
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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