Holter-Hausner Intl. - FDA 510(k) Cleared Devices
42
Total
38
Cleared
0
Denied
Holter-Hausner Intl. has 38 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 38 cleared submissions from 1978 to 1988. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Holter-Hausner Intl. Filter by specialty or product code using the sidebar.
42 devices
Cleared
Jul 14, 1988
H-H FLUSHING RESERVOIR
Neurology
198d
Cleared
Jan 19, 1988
H-H EXTERNAL VENTRICULAR DRAINAGE COLLECTION BAG
Neurology
78d
Cleared
Sep 28, 1987
H-H HUNTER ACTIVE TENDON IMPLANT PC
Orthopedic
104d
Cleared
Sep 28, 1987
H-H HUNTER ACTIVE TENDON IMPLANT DC
Orthopedic
104d
Cleared
Sep 28, 1987
H-H HUNTER ACTIVE TENDON IMPLANT BC
Orthopedic
104d
Cleared
May 14, 1987
H-H HARRIS NEONATAL NASAL CANNULA SET FOR CPAP
Anesthesiology
38d
Cleared
May 01, 1987
H-H EXTERNAL VENTRICULAR DRAIN (EVD) COMP./SYSTEMS
Neurology
71d
Cleared
Jan 13, 1987
H-H SUBGALEAL TROCAR
Neurology
15d
Cleared
Oct 16, 1985
H-H HUNTER PASSIVE TENDON IMPLANT
General & Plastic Surgery
62d
Cleared
Oct 16, 1985
H-H HUNTER TENDON ROD
Orthopedic
62d
Cleared
Sep 30, 1985
H-H HUNTER ACTIVE TENDON IMPLANT
Orthopedic
46d
Cleared
Sep 18, 1985
H-H CATHETER PASSERS(TACL DESIGN
Neurology
37d
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