510(k) K801887
K801887 is an FDA 510(k) premarket notification submitted by Aesculap Instruments Corp. for the device "DRILL, DENTAL". The FDA issued a decision of Substantially Equivalent on August 20, 1980. The device falls under product code DZA (Drill, Dental, Intraoral), a Class I device regulated under 21 CFR 872.4130. Aesculap Instruments Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 20, 1980
- Date Received
- July 28, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Drill, Dental, Intraoral
- Device Class
- Class I
- Regulation Number
- 872.4130
- Review Panel
- DE
- Submission Type