Medical Device Manufacturer · US , Danvers , MA

Keta Corp. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1984
3
Total
3
Cleared
0
Denied

FDA 510(k) Regulatory Record - Keta Corp. Ophthalmic ✕

3 devices
1-3 of 3
Cleared May 06, 1986
KETA HAND-HELD TONOMETER
K861027 · HKS
Ophthalmic · 49d
Cleared Apr 04, 1986
SUPERLITE PENLIGHT
K861028
Ophthalmic · 17d
Cleared Dec 05, 1984
QUANTUM 412
K844570 · HPT
Ophthalmic · 12d
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