510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K931379Substantially Equivalent

Microvasive Insurg Laptie Suture Ligator

Boston Scientific Corporation, San Jose CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K931379 is the FDA 510(k) clearance record for MICROVASIVE INSURG LAPTIE SUTURE LIGATOR, a class I device, cleared for Boston Scientific Corp on under FDA product code HCF (Instrument, Ligature Passing And Knot Tying). FDA records list 1,110 510(k) clearances for Boston Scientific Corp, from to . As of , FDA records show no recalls naming K931379.

Clearance record

Decision date
Received
(117 days to decision)
Product code
HCF Instrument, Ligature Passing And Knot Tying
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Boston Scientific Corp 2710 Orchard Pkwy., San Jose CA
510(k) summary
Summary
Third party review
No

Clearances, product code HCF

Trailing 12 months

FDA records hold no clearances under product code HCF in the trailing twelve months.

FDA records show no clearances under product code HCF in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HCF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260