510(k) K863912

THE MMG 5 IN 1 CONNECTOR by Medical Marketing Group — Product Code BYX

K863912 is an FDA 510(k) premarket notification submitted by Medical Marketing Group for the device "THE MMG 5 IN 1 CONNECTOR". The FDA issued a decision of Substantially Equivalent on October 27, 1986. The device falls under product code BYX (Tubing, Pressure And Accessories), a Class I device regulated under 21 CFR 868.5860. Medical Marketing Group has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 27, 1986
Date Received
October 8, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tubing, Pressure And Accessories
Device Class
Class I
Regulation Number
868.5860
Review Panel
AN
Submission Type