Product code GIO— Hematology
CAPILLARY BLOOD COLLECTION TUBE
- Classification name
- Tube, Collection, Capillary Blood
- Device class
- Class 1
- Regulation
- 21 CFR 864.6150
- Advisory panel
- Hematology
- Total cleared
- 22
- First cleared
- Most recent
Market context for product code GIO
FDA has cleared devices under product code GIO between 1977 and 1997, 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
- 1997
- 1994
- 1989
- 1988
- 1987
- 1985
- 1984
- 1983
- 1981
- 1977
Top applicants under product code GIO
Recent clearances under product code GIO
- K972969 — QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEM
- K941291 — MONOJECT SAMPLETTE SEPARATOR TUBE
- K894851 — TRU-TRAX
- K885324 — HEMA(PRO)TEC(TION)
- K885138 — CAPILLARY TUBE, BLOOD COLLECTION
- K884623 — SAFE-TEC CAPILLARY BLOOD COLLECTION TUBE
- K881187 — NATELSON TUBES, HEPARIN AND PLAIN
- K881262 — CARAWAY TUBES, HEPARIN AND PLAIN
- K875061 — MONOJECT SAMPLETTE AMBER CAPILLARY SERUM SEPARATOR
- K873647 — VENTRESCREEN CAPILLARY BLOOD COLLECTION TUBE
- K850806 — CORNING BLOOD COLLECTION CAPILLARY TUBES
- K843608 — CAPILLARY BLOOD COLLECTION TUBE
- K843892 — MICRO HEMATOCRIT CAPILLARY TUBES
- K843361 — MINICAPS
- K843362 — RINGCAPS
- K832578 — MONOJET SAMPLETTE ADAPTERS
- K812921 — S/P SURE-CAP
- K812922 — S/P SURE-CAP C
- K812923 — S/P SURE-CAP N
- K812969 — S/P CAPILLARY TUBES, HEPARINIZED (2A)
- K812970 — S/P CAPILLARY TUBES, HEPARINIZED (3A)
- K770981 — LANCER CAPILLARY BLOOD SERUM SEPARATOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.