The following data is part of a premarket notification filed by Young Dental Manufacturing Co 1, Llc. with the FDA for Prophylaxis Angle.
Device ID | K790722 |
510k Number | K790722 |
Device Name: | PROPHYLAXIS ANGLE |
Classification | Handpiece, Contra- And Right-angle Attachment, Dental |
Applicant | YOUNG DENTAL MANUFACTURING CO 1, LLC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | EGS |
CFR Regulation Number | 872.4200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1979-04-10 |
Decision Date | 1979-06-15 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
10302732826123 | K790722 | 000 |
10302732824129 | K790722 | 000 |
10302732816124 | K790722 | 000 |
10302732814120 | K790722 | 000 |
10302730001898 | K790722 | 000 |