The following data is part of a premarket notification filed by Storz Instrument Co. with the FDA for Storz Dp4310deluxe Phaco Pack Without Reflux.
| Device ID | K955901 |
| 510k Number | K955901 |
| Device Name: | STORZ DP4310DELUXE PHACO PACK WITHOUT REFLUX |
| Classification | Unit, Phacofragmentation |
| Applicant | STORZ INSTRUMENT CO. 3365 TREE CT. INDUSTRIAL BLVD. St. Louis, MO 63122 -6694 |
| Contact | Audrey Swearingen |
| Correspondent | Audrey Swearingen 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 | 1995-12-29 |
| Decision Date | 1996-03-28 |
| Summary: | summary |