Shiley Cricothyrotomy Tube
FDA 510(k) K781639 · Shiley, Inc.
510(k) numberK781639
Submission
- Device name
- Shiley Cricothyrotomy Tube
- Applicant
- Shiley, Inc.
Mchenry, IL, US - Received
- September 21, 1978
- Decision date
- October 24, 1978
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- EQN – Laryngoscope, Nasopharyngoscope
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 874.4760
- Specialty
- Ear, Nose, Throat
If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).
Other 510(k)s with product code EQN
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K252624 | KARL STORZ Laryngoscopes and AccessoriesEQN · Traditional | KARL STORZ Endoscopy-America, Inc. | 05/15/2026SE |
| K150248 | ORL Video NasoPharyngo-LarngoscopeEQN · Traditional | Jedmed Instrument Company | 07/23/2015SE |
| K132039 | Ergo-Flex Laryngo-Nasopharyngoscope Ef-N and Ef-N SlimEQN · Traditional | Jedmed Instrument Co. | 02/21/2014SE |
| K834172 | Op-Con Surg. Instrument #7EQN · Traditional | Imm Enterprises , Ltd. | 03/06/1984SE |
| K831255 | Laryngoscope Attachment PH2000EQN · Traditional | Eder Instrument Co, Inc. | 09/12/1983SE |
| K830888 | Cool-Lite Fibercoptic Laryngeal ExamEQN · Traditional | National Medical Technology | 04/27/1983SE |
| K822525 | Laryngoscopes RigidEQN · Traditional | Kelleher Corp. | 09/09/1982SE |
| K821710 | Nagashima NX-150F Light Source UnitEQN · Traditional | Kelleher Corp. | 06/25/1982SE |
| K821709 | Nagashima Light Source Unit SL-5EQN · Traditional | Kelleher Corp. | 06/25/1982SE |
| K821708 | Nagashima Light Source Unit SL-4EQN · Traditional | Kelleher Corp. | 06/25/1982SE |
More from Kelleher Corp.
| 510(k) | Device | Decision |
|---|---|---|
| K920594 | Shiley Perfusion Tubing SetsDTM · Traditional | 03/18/1993SE |
| K910991 | Shiley Therapeutic Autotransfusion SystemCAC · Traditional | 11/27/1991SE |
| K911876 | Shiley Plexus(R) Venous Reservoir, PVR1200DTN · Traditional | 08/09/1991SE |
| K910923 | BCD AdvancedDTR · Traditional | 04/09/1991SE |
| K901548 | Biomedical Sensors-Shiley BGM 4000 Intra Blood GasCCC · Traditional | 01/14/1991SE |
| K903435 | Shiley Specialized Tracheostomy TubeJOH · Traditional | 10/02/1990SE |
| K901624 | Shiley Plexus Integral Reservoir Hollow Fiber Oxy.DTZ · Traditional | 07/03/1990SE |
| K901250 | Plexus 2(TM) Infant Hollow Fiber OxygenatorDTZ · Traditional | 06/11/1990SE |
| K901249 | Plexus 3.5(TM) Pediatric Hollow Fiber OxygenatorDTZ · Traditional | 06/11/1990SE |
| K900797 | Stockert Shiley Dual Pressure Control Module XRDXS · Traditional | 05/10/1990SE |
Questions and answers
When was Shiley Cricothyrotomy Tube cleared by the FDA?
Shiley Cricothyrotomy Tube (K781639) received a 510(k) decision of Substantially Equivalent on October 24, 1978, 33 days after the submission was received.
What is the product code of K781639?
The FDA product code is EQN – Laryngoscope, Nasopharyngoscope, a Class II (moderate risk) device regulated under 21 CFR 874.4760.