510(k) K163537
K163537 is an FDA 510(k) premarket notification submitted by Covidien, LLC for the device "Arcpoint pulmonary needle - 18 ga, Arcpoint pulmonary needle - 21 ga". The FDA issued a decision of Substantially Equivalent on Apr 21, 2017. The device falls under product code EOQ (Bronchoscope (Flexible Or Rigid)), a Class II device regulated under 21 CFR 874.4680. Covidien, LLC has 224 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 21, 2017
- Date Received
- Dec 16, 2016
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Bronchoscope (Flexible Or Rigid)
- Device Class
- Class II
- Regulation Number
- 874.4680
- Review Panel
- EN
- Submission Type
- 510(k)
A bronchoscope (flexible or rigid) and accessories is a tubular endoscopic device with any of a group of accessory devices which attach to the bronchoscope and is intended to examine or treat the larynx and tracheobronchial tree. If the device is reprocessed, reprocessing validation data for this device type must be included in a 510(k) submission. 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).