Product code EHZ— Dental
AUTO-RINSE
- Classification name
- Evacuator, Oral Cavity
- Device class
- Class 1
- Regulation
- 21 CFR 872.6640
- Advisory panel
- Dental
- Total cleared
- 17
- First cleared
- Most recent
Market context for product code EHZ
FDA has cleared devices under product code EHZ between 1977 and 1997, filed by 15 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
- 1997
- 1994
- 1991
- 1990
- 1989
- 1988
- 1987
- 1986
- 1980
- 1979
- 1978
- 1977
Top applicants under product code EHZ
Recent clearances under product code EHZ
- K973248 — IMTEC BONE COLLECTOR SYSTEM
- K941164 — TAP EXPRESS EJECTOR
- K911072 — SUPER EVACRETRACTOR, DISPOSABLE ORAL EVACUATOR
- K903718 — OROSCOPE MODEL NUMBER COS-100
- K892881 — DENTAL SANI-SLEEVE STERILE 60MM X 1650MM #1101
- K892882 — DENTAL SANI-SLEEVE STERILE 100MM X 2200MM #1102
- K880754 — DRI-CLAVE LIQUID KLEENZALL
- K873545 — PORTABLE FIELD DENTAL OPERATING & TREATMENT UNIT
- K874401 — TITANIUM SUCTION TIP
- K864621 — VAC - RITE RIGHT ANGLE ASPIRATOR TUBE & HOLDER
- K863769 — EVACUATOR TIPS
- K801682 — SPACELINE HIGH VOLUME EVACUATION HANDPIE
- K782068 — MVS UNIT, MODEL SEU-8 AND DEU-8, 80
- K781486 — STERI-VAC POWER UNITS
- K781488 — MVS-MODEL SEU-6, DEU-6
- K780701 — DENTAL OFFICE ENVIRONMENT CONTROL UNIT
- K770152 — AUTO-RINSE
Data sourced from openFDA. This site is unofficial and independent of the FDA.