510(k) K821769
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