The following data is part of a premarket notification filed by H&h Instruments with the FDA for Hhi Pneumatic Rotary Drill.
Device ID | K922661 |
510k Number | K922661 |
Device Name: | HHI PNEUMATIC ROTARY DRILL |
Classification | Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/attachment |
Applicant | H&H INSTRUMENTS 4950 CRESCENT TECHNICAL CT St Augustine, FL 32086 |
Contact | Mary K Horvath |
Correspondent | Mary K Horvath H&H INSTRUMENTS 4950 CRESCENT TECHNICAL CT St Augustine, FL 32086 |
Product Code | HSZ |
CFR Regulation Number | 878.4820 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-06-03 |
Decision Date | 1992-09-18 |