The following data is part of a premarket notification filed by Quest Medical, Inc. with the FDA for Lacricath Lacrimal Duct Catheter.
| Device ID | K113867 |
| 510k Number | K113867 |
| Device Name: | LACRICATH LACRIMAL DUCT CATHETER |
| Classification | Lacrimal Stents And Intubation Sets |
| Applicant | QUEST MEDICAL, INC. ONE ALLENTOWN PKWY. Allen, TX 75002 |
| Contact | Amy Clendening-wheeler |
| Correspondent | Amy Clendening-wheeler QUEST MEDICAL, INC. ONE ALLENTOWN PKWY. Allen, TX 75002 |
| Product Code | OKS |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-12-30 |
| Decision Date | 2012-10-19 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20634624438525 | K113867 | 000 |
| 20634624438518 | K113867 | 000 |
| 20634624438327 | K113867 | 000 |
| 20634624438310 | K113867 | 000 |
| 20634624438228 | K113867 | 000 |
| 20634624438211 | K113867 | 000 |