Product code KCB
- Device name
- Tube, Tonsil Suction
- Medical specialty
- Ear, Nose, Throat
- Device class
- 1
- Regulation number
- 874.4420
- Review panel
- EN
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset
Related 510(k) Records#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K801468 | FRAZIER-FERGUSON SUCTION TUBES | Edward Weck, Inc. | 1980-08-12 |
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| 00840183532635 | BR Surgical, LLC | BR Surgical, LLC | 2026-07-16 |
| 08906039315110 | OSSEOUS Suction tubes for Throat | EON MEDITECH PRIVATE LIMITED | 2024-06-25 |
| 08904461011198 | OSSEOUS Suction tubes for Throat | EON MEDITECH PRIVATE LIMITED | 2024-06-25 |
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| 10381780538424 | MicroFrance® | INTEGRA MICROFRANCE | 2024-05-29 |
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| G586G109493NC0 | Novo Surgical | NOVO SURGICAL, INC. | 2024-02-22 |
| G586G109489NC0 | Novo Surgical | NOVO SURGICAL, INC. | 2024-02-22 |
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| G043106010 | BEAR | Bear-Ent, LLC | 2022-10-13 |
| 10889942605118 | Medline Industries, Inc. | MEDLINE INDUSTRIES, INC. | 2022-08-04 |