510(k) K863561

URESIL THORACIC VENT by Uresil Corp. — Product Code KDQ

K863561 is an FDA 510(k) premarket notification submitted by Uresil Corp. for the device "URESIL THORACIC VENT". The FDA issued a decision of Substantially Equivalent on September 23, 1986. The device falls under product code KDQ (Bottle, Collection, Vacuum), a Class II device regulated under 21 CFR 880.6740. Uresil Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 23, 1986
Date Received
September 12, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bottle, Collection, Vacuum
Device Class
Class II
Regulation Number
880.6740
Review Panel
HO
Submission Type