Vitalograph, Inc.

FDA Regulatory Profile

Vitalograph, Inc. appears in FDA public data with 0 recalls, 22 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Dec 3, 2025.

Summary

Total Recalls
0
510(k) Clearances
22
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253293VitaloJAK Clinic (Model 7100)Dec 3, 2025
K000599VITALOGRAPH BASE STATIONSep 8, 2000
K991412VITALOGRAPH MICROFeb 4, 2000
K943678ELECTRONIC FLOW METERDec 14, 1995
K950854VITALOGRAPH 2110 SOFTWARE INTERFACEOct 12, 1995
K946075VITALOGRAPH MODEL 2120Aug 4, 1995
K942779DISPOSABLE BACTERIOLOGICAL FILTERJul 13, 1994
K925085ESCORT SPIROMETERAug 12, 1993
K930085VITALOGRAPH DATA STORAGE SPIROMETERJul 26, 1993
K912412VITALOGRAPH SPIROTRAC IIIOct 15, 1991
K893665AEROSOL INHALATION MONITORAug 21, 1989
K892524VITALOGRAPH-BREATHCO MONITORMay 5, 1989
K873562VITALOGRAPH-ALPHAAug 29, 1988
K874892VITALOGRAPH-EC60 HYDROGEN MONITORJun 2, 1988
K863420VITALOGRAPH EC-50 CARBON MONOXIDE MONITORJan 15, 1987
K860949DUAL-AIDMay 6, 1986
K854526VITALOGRAPH COMPACTDec 24, 1985
K844963VITAPEPJun 7, 1985
K833785EMERGENCY ASPIRATORDec 22, 1983
K823683VITALOGRAPH PFT PRINTERJan 21, 1983