510(k) K822197

NEEDLE HOLDERS by Kelleher Corp. — Product Code LCR

K822197 is an FDA 510(k) premarket notification submitted by Kelleher Corp. for the device "NEEDLE HOLDERS". The FDA issued a decision of Substantially Equivalent on August 16, 1982. The device falls under product code LCR (Fluorescent Immunoassay, Tobramycin), a Class II device regulated under 21 CFR 862.3900. Kelleher Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 16, 1982
Date Received
July 23, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Fluorescent Immunoassay, Tobramycin
Device Class
Class II
Regulation Number
862.3900
Review Panel
TX
Submission Type