The following data is part of a premarket notification filed by Trokamed Gmbh with the FDA for Trokamed Gmbh Endoscopes And Accessories.
| Device ID | K060233 |
| 510k Number | K060233 |
| Device Name: | TROKAMED GMBH ENDOSCOPES AND ACCESSORIES |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | TROKAMED GMBH KLEINE BREITE 17 Geisingen, DE 78187 |
| Contact | Karlheinz Trondle |
| Correspondent | Karlheinz Trondle TROKAMED GMBH KLEINE BREITE 17 Geisingen, DE 78187 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-01-30 |
| Decision Date | 2006-07-19 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| M27463045201 | K060233 | 000 |
| M2746303401 | K060233 | 000 |
| M2746003401 | K060233 | 000 |
| M2746003221 | K060233 | 000 |
| M2746003201 | K060233 | 000 |
| M2746152121 | K060233 | 000 |
| M27460030521 | K060233 | 000 |
| M27460030511 | K060233 | 000 |
| M27460030291 | K060233 | 000 |
| M27460030271 | K060233 | 000 |
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| M27460030171 | K060233 | 000 |
| M27460030051 | K060233 | 000 |
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| M2746304271 | K060233 | 000 |
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| M27460045041 | K060233 | 000 |
| M274600448KNR1 | K060233 | 000 |
| M2746004481 | K060233 | 000 |
| M27460042631 | K060233 | 000 |
| M274600340HOUS1 | K060233 | 000 |
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| M274505SPR2301 | K060233 | 000 |
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| M2745052311 | K060233 | 000 |
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| M27463233081 | K060233 | 000 |