510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K911913Substantially Equivalent

Precision Glide - Enhanced Surgical Blade

BD Becton Dickinson Vacutainer Systems Preanalytic, Franklin Lakes NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K911913 is the FDA 510(k) clearance record for PRECISION GLIDE - ENHANCED SURGICAL BLADE, a class I device, cleared for Bd Becton Dickinson Vacutainer Systems Preanalytic on under FDA product code GES (Blade, Scalpel). FDA records list 632 510(k) clearances for Bd Becton Dickinson Vacutainer Systems Preanalytic, from to . As of , FDA records show no recalls naming K911913.

Clearance record

Decision date
Received
(13 days to decision)
Product code
GES Blade, Scalpel
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic 1 Becton Dr., Franklin Lakes NJ
510(k) summary
Statement
Third party review
No

Clearances, product code GES

Trailing 12 months

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

FDA records show no clearances under product code GES in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GES, 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