510(k) K791532

SURELOC EXTERNAL CONNECTOR by Polamedco, Inc. — Product Code BZA

K791532 is an FDA 510(k) premarket notification submitted by Polamedco, Inc. for the device "SURELOC EXTERNAL CONNECTOR". The FDA issued a decision of Substantially Equivalent on September 4, 1979. The device falls under product code BZA (Connector, Airway (Extension)), a Class I device regulated under 21 CFR 868.5810. Polamedco, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 4, 1979
Date Received
August 10, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Connector, Airway (Extension)
Device Class
Class I
Regulation Number
868.5810
Review Panel
AN
Submission Type