The following data is part of a premarket notification filed by Storz Instrument Co. with the FDA for Storz Phaco And Frag Handpieces.
Device ID | K935926 |
510k Number | K935926 |
Device Name: | STORZ PHACO AND FRAG HANDPIECES |
Classification | Unit, Phacofragmentation |
Applicant | STORZ INSTRUMENT CO. 3365 TREE CT. INDUSTRIAL BLVD. St. Louis, MO 63122 -6694 |
Contact | Micheal H Southworth |
Correspondent | Micheal H Southworth STORZ INSTRUMENT CO. 3365 TREE CT. INDUSTRIAL BLVD. St. Louis, MO 63122 -6694 |
Product Code | HQC |
CFR Regulation Number | 886.4670 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-12-13 |
Decision Date | 1994-11-28 |