510(k) K833608

GOLD ALLIGATOR FORCEPS by Microtek Medical, Inc. — Product Code KAE

K833608 is an FDA 510(k) premarket notification submitted by Microtek Medical, Inc. for the device "GOLD ALLIGATOR FORCEPS". The FDA issued a decision of Substantially Equivalent on January 11, 1984. The device falls under product code KAE (Forceps, Ent), a Class I device regulated under 21 CFR 874.4420. Microtek Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 11, 1984
Date Received
October 12, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Forceps, Ent
Device Class
Class I
Regulation Number
874.4420
Review Panel
EN
Submission Type