510(k) K905130

FETAL MONITORING SPIRAL ELECTRODE by Graphic Controls Corp. — Product Code HGP

K905130 is an FDA 510(k) premarket notification submitted by Graphic Controls Corp. for the device "FETAL MONITORING SPIRAL ELECTRODE". The FDA issued a decision of Substantially Equivalent on January 29, 1991. The device falls under product code HGP (Electrode, Circular (Spiral), Scalp And Applicator), a Class II device regulated under 21 CFR 884.2675. Graphic Controls Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 29, 1991
Date Received
November 15, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrode, Circular (Spiral), Scalp And Applicator
Device Class
Class II
Regulation Number
884.2675
Review Panel
OB
Submission Type