510(k) K803174
K803174 is an FDA 510(k) premarket notification submitted by Conphar, Inc. for the device "CONPHAR PERCUSSION HAMMER(BUCK TYPE)". The FDA issued a decision of Substantially Equivalent on Dec 30, 1980. The device falls under product code GWZ (Percussor), a Class I device regulated under 21 CFR 882.1700. Conphar, Inc. has 121 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 30, 1980
- Date Received
- Dec 15, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Percussor
- Device Class
- Class I
- Regulation Number
- 882.1700
- Review Panel
- NE
- Submission Type
- 510(k) Exempt