510(k) K931379
K931379 is an FDA 510(k) premarket notification submitted by Boston Scientific Corp for the device "MICROVASIVE INSURG LAPTIE SUTURE LIGATOR". The FDA issued a decision of Substantially Equivalent on July 13, 1993. The device falls under product code HCF (Instrument, Ligature Passing And Knot Tying), a Class I device regulated under 21 CFR 878.4800. Boston Scientific Corp has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 13, 1993
- Date Received
- March 18, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Instrument, Ligature Passing And Knot Tying
- Device Class
- Class I
- Regulation Number
- 878.4800
- Review Panel
- SU
- Submission Type