510(k) K821769

MICROKNIFE by Biological & Environmental Control Laboratories — Product Code EMF

K821769 is an FDA 510(k) premarket notification submitted by Biological & Environmental Control Laboratories for the device "MICROKNIFE". The FDA issued a decision of Substantially Equivalent on September 14, 1982. The device falls under product code EMF (Knife, Surgical), a Class I device regulated under 21 CFR 878.4800. Biological & Environmental Control Laboratories has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 14, 1982
Date Received
June 10, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Knife, Surgical
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type