510(k) K930760

MED-PLASTICS INTL., INC. BREATHING FILTER by Med-Plastics Intl., Inc. — Product Code CAH

K930760 is an FDA 510(k) premarket notification submitted by Med-Plastics Intl., Inc. for the device "MED-PLASTICS INTL., INC. BREATHING FILTER". The FDA issued a decision of Substantially Equivalent on March 11, 1993. The device falls under product code CAH (Filter, Bacterial, Breathing-Circuit), a Class II device regulated under 21 CFR 868.5260. Med-Plastics Intl., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 11, 1993
Date Received
February 12, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Filter, Bacterial, Breathing-Circuit
Device Class
Class II
Regulation Number
868.5260
Review Panel
HO
Submission Type