The following data is part of a premarket notification filed by Hollister, Inc. with the FDA for Hollister Feeding Tube Attachment Device.
| Device ID | K893888 |
| 510k Number | K893888 |
| Device Name: | HOLLISTER FEEDING TUBE ATTACHMENT DEVICE |
| Classification | Tubes, Gastrointestinal (and Accessories) |
| Applicant | HOLLISTER, INC. 2000 HOLLISTER DR. Libertyville, IL 60048 |
| Contact | Sharon Leaf |
| Correspondent | Sharon Leaf HOLLISTER, INC. 2000 HOLLISTER DR. Libertyville, IL 60048 |
| Product Code | KNT |
| CFR Regulation Number | 876.5980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-05-30 |
| Decision Date | 1989-10-17 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10610075167767 | K893888 | 000 |