Medical Device Manufacturer · CA , Montreal, Qc.

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

13 submissions · 13 cleared · Since 1991

Total

Cleared

Denied

Octostop, Inc. has 13 FDA 510(k) cleared radiology devices. Based in Montreal, Qc., CA.

Historical record: 13 cleared submissions from 1991 to 1997.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Octostop, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Octostop, Inc.

13 devices

1-13 of 13

Cleared Aug 14, 1997

PIVOTING COMPENSATING FILTERS FOR THE HEAD

K972766 · KPR

Radiology · 21d

Cleared Nov 27, 1996

THE PHARAOH COMPENSATING FILTER

OCTOSTOP COMPENSATING FILTERS

K940306 · KPR

Radiology · 237d

Cleared Sep 02, 1994

OCTOSTOP(R) CHAIR (NEW MODEL

K935444 · IXR

Radiology · 294d

Cleared Feb 09, 1994

VARIANT OF OCTOSTOP AND OCTOPAQUE

K930124 · KXH

Radiology · 393d

Cleared Jul 13, 1993

ACCESSORY TO UNIVERSAL OCTOPAQUE

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

FDA 510(k) Regulatory Record - Octostop, Inc.

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