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
K851102Substantially Equivalent

Vasoscreen Impedance Plethysmograph

Sonicaid, Inc., Fredericksburg VA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K851102 is the FDA 510(k) clearance record for VASOSCREEN IMPEDANCE PLETHYSMOGRAPH, a class II device, cleared for Sonicaid, Inc. on under FDA product code DQB (Phlebograph, Impedance). FDA records list 18 510(k) clearances for Sonicaid, Inc., from to . As of , FDA records show no recalls naming K851102.

Clearance record

Decision date
Received
(58 days to decision)
Product code
DQB Phlebograph, Impedance
Regulation
21 CFR 870.2750
Device class
Class II
Review panel
Cardiovascular
Applicant
Sonicaid, Inc. P.O. Box 588, Fredericksburg VA
Third party review
No

Clearances, product code DQB

Trailing 12 months

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

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