510(k) K841871

LIQUA-SONIC GEL by Chester Labs, Inc. — Product Code GYB

K841871 is an FDA 510(k) premarket notification submitted by Chester Labs, Inc. for the device "LIQUA-SONIC GEL". The FDA issued a decision of Substantially Equivalent on March 14, 1985. The device falls under product code GYB (Media, Electroconductive), a Class II device regulated under 21 CFR 882.1275. Chester Labs, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 14, 1985
Date Received
May 7, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Media, Electroconductive
Device Class
Class II
Regulation Number
882.1275
Review Panel
NE
Submission Type