Product code JAC— Radiology
ADMARK
- Classification name
- System, X-Ray, Film Marking, Radiographic
- Device class
- Class 1
- Regulation
- 21 CFR 892.1640
- Advisory panel
- Radiology
- Total cleared
- 18
- First cleared
- Most recent
Market context for product code JAC
FDA has cleared devices under product code JAC between 1985 and 1994, filed by 13 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1994
- 1993
- 1992
- 1991
- 1989
- 1988
- 1987
- 1985
Top applicants under product code JAC
Recent clearances under product code JAC
- K942883 — DIGITAL I.D. CAMERA
- K930752 — CT/MRI TOPOGRAPHIC MARKER
- K932357 — FUJI EC ID CAMERA
- K925892 — SOLSTICE XRAY RING MARKER PAD
- K923533 — ADMARK
- K926404 — KODAK X-OMATIC IDENTIFICATION CAMERA, MODEL 4 & 4L
- K924345 — RADIOGRAPHIC FILM MARKETING SYSTEM
- K925332 — BENNETT X-RAY ID PLUS
- K920031 — KODAK X-OMATIC IDENT. CAMERA MAMMOGRAPHY UPGRADE
- K915088 — KODAK MIN-R IDENTIFICATION CAMERA
- K913478 — RADIOGRAPHIC FILM MARKING SYSTEM
- K911873 — X-MARX
- K910354 — DU PONT IDENTIFICATION CAMERA
- K890467 — KODAK PORTABLE IDENTIFICATION CAMERA
- K882519 — X-RAY MARKER
- K870565 — KODAK X-OMATIC IDENT. CAMERA, MODELS 2 AND 2L
- K870701 — KODAK X-OMATIC IDENTIFICATION CAMERA DIGITAL
- K852160 — RADIOLOGICAL MARKING PEN
Data sourced from openFDA. This site is unofficial and independent of the FDA.