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
K860030Substantially Equivalent

Surgidyne Varidyne, Model 140-2I & Model 140-2Id

Surgidyne, Inc., Eden Prairie MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K860030 is the FDA 510(k) clearance record for SURGIDYNE VARIDYNE, MODEL 140-2I & MODEL 140-2ID, a class II device, cleared for Surgidyne, Inc. on under FDA product code BTA (Pump, Portable, Aspiration (Manual Or Powered)). FDA records list 6 510(k) clearances for Surgidyne, Inc., from to . As of , FDA records show no recalls naming K860030.

Clearance record

Decision date
Received
(37 days to decision)
Product code
BTA Pump, Portable, Aspiration (Manual Or Powered)
Regulation
21 CFR 878.4780
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Surgidyne, Inc. 9600 W. 76th St., Suite D, Eden Prairie MN
Third party review
No

Clearances, product code BTA

Trailing 12 months
6 clearances under product code BTA in the twelve months to October 2026, May 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code BTA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20261
May 20264
June 20260
July 20260
August 20260
September 20260
October 20260