The following data is part of a premarket notification filed by Storz Instrument Co. with the FDA for Storz Fiberoptic Endo-illuminators.
| Device ID | K896549 |
| 510k Number | K896549 |
| Device Name: | STORZ FIBEROPTIC ENDO-ILLUMINATORS |
| Classification | Illuminator, Fiberoptic, Surgical Field |
| Applicant | STORZ INSTRUMENT CO. 3365 TREE CT. INDUSTRIAL BLVD. St. Louis, MO 63122 -6694 |
| Contact | Dan Regan |
| Correspondent | Dan Regan STORZ INSTRUMENT CO. 3365 TREE CT. INDUSTRIAL BLVD. St. Louis, MO 63122 -6694 |
| Product Code | HBI |
| CFR Regulation Number | 878.4580 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-11-17 |
| Decision Date | 1990-02-15 |