510(k) K990561
K990561 is an FDA 510(k) premarket notification submitted by Pilling Weck Surgical for the device "OPTICAL FORCEPS". The FDA issued a decision of Substantially Equivalent on May 14, 1999. The device falls under product code JEK (Forceps, Biopsy, Bronchoscope (Rigid)), a Class II device regulated under 21 CFR 874.4680. Pilling Weck Surgical has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 14, 1999
- Date Received
- February 22, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Forceps, Biopsy, Bronchoscope (Rigid)
- Device Class
- Class II
- Regulation Number
- 874.4680
- Review Panel
- EN
- Submission Type
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).