510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K843591Substantially Equivalent

Intercept

Vital Signs, Inc., East Rutherford NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K843591 is the FDA 510(k) clearance record for INTERCEPT, a class II device, cleared for Vital Signs, Inc. on under FDA product code KDP (Regulator, Vacuum). FDA records list 75 510(k) clearances for Vital Signs, Inc., from to . As of , FDA records show no recalls naming K843591.

Clearance record

Decision date
Received
(37 days to decision)
Product code
KDP Regulator, Vacuum
Regulation
21 CFR 880.6740
Device class
Class II
Review panel
General Hospital
Applicant
Vital Signs, Inc. 1 Madison St., East Rutherford NJ
Third party review
No

Clearances, product code KDP

Trailing 12 months

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

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