510(k) K980530
K980530 is an FDA 510(k) premarket notification submitted by Peregrine Surgical , Ltd. for the device "PEREGRINE FIBER OPTIC BIPOLAR STRAIGHT PICK AND ANGLED PICK, MODELS PD100.12 AND PD100.13". The FDA issued a decision of Substantially Equivalent on May 12, 1998. The device falls under product code MPA (Endoilluminator), a Class II device regulated under 21 CFR 876.1500. Peregrine Surgical , Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 12, 1998
- Date Received
- February 11, 1998
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Endoilluminator
- Device Class
- Class II
- Regulation Number
- 876.1500
- Review Panel
- OP
- Submission Type