510(k) K841005
K841005 is an FDA 510(k) premarket notification submitted by Premier Dental Products Co. for the device "TONSIL KNIFE-VARIOUS". The FDA issued a decision of Substantially Equivalent on May 30, 1984. The device falls under product code KBQ (Knife, Tonsil), a Class I device regulated under 21 CFR 874.4420. Premier Dental Products Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 30, 1984
- Date Received
- March 9, 1984
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Knife, Tonsil
- Device Class
- Class I
- Regulation Number
- 874.4420
- Review Panel
- EN
- Submission Type