510(k) K912558

GULL ELISAWARE by Gull Laboratories, Inc. — Product Code LIB

K912558 is an FDA 510(k) premarket notification submitted by Gull Laboratories, Inc. for the device "GULL ELISAWARE". The FDA issued a decision of Substantially Equivalent on September 16, 1991. The device falls under product code LIB (Device, General Purpose, Microbiology, Diagnostic), a Class I device regulated under 21 CFR 866.2660. Gull Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 16, 1991
Date Received
June 11, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, General Purpose, Microbiology, Diagnostic
Device Class
Class I
Regulation Number
866.2660
Review Panel
MI
Submission Type