Medical Device Manufacturer · US , Winfield , MO

Syntec, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1997
3
Total
3
Cleared
0
Denied

FDA 510(k) Regulatory Record - Syntec, Inc. Ophthalmic ✕

3 devices
1-3 of 3
Cleared Jan 04, 2001
PHACOGARD
K002932 · HQC
Ophthalmic · 106d
Cleared May 04, 1998
SYNTEC VITMAN
K980480 · HQC
Ophthalmic · 90d
Cleared May 06, 1997
SYNTEC, INC. DISPOSABLE BARE END FIBER
K971338 · MPA
Ophthalmic · 26d
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