The following data is part of a premarket notification filed by Surgitek Medical Engineering Corp. with the FDA for Sclerotherapy Needle.
| Device ID | K914496 |
| 510k Number | K914496 |
| Device Name: | SCLEROTHERAPY NEEDLE |
| Classification | Endoscopic Injection Needle, Gastroenterology-urology |
| Applicant | SURGITEK MEDICAL ENGINEERING CORP. 3037 MT. PLEASANT ST. Racine, WI 53404 |
| Contact | Brian Kunst |
| Correspondent | Brian Kunst SURGITEK MEDICAL ENGINEERING CORP. 3037 MT. PLEASANT ST. Racine, WI 53404 |
| Product Code | FBK |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-10-08 |
| Decision Date | 1991-12-05 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00821925001299 | K914496 | 000 |