THE PHARAOH COMPENSATING FILTER— 510(k) K963941

Name: FDA 510(k) clearance K963941
Creator: U.S. Food and Drug Administration
Published: 1996-11-27

Substantially Equivalent

Octostop, Inc.

FDA 510(k) clearance K963941 for THE PHARAOH COMPENSATING FILTER, Substantially Equivalent on 1996-11-27. Applicant: Octostop, Inc.. Device class: 2.

Clearance details

Applicant: Octostop, Inc.
Product code: Code KPR
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 1996-10-01
Decision date: 1996-11-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montreal, Qc., CA

Download summary PDF View on FDA.gov ↗

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K260481 — GC85A2026-08-27
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K253446 — AeroDR TX c022026-04-10

More clearances from Octostop, Inc.

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K972766 — PIVOTING COMPENSATING FILTERS FOR THE HEAD1997-08-14
K953246 — OCTOROLL1995-09-29
K952871 — RIDGES PLUS1995-07-20
K942916 — OCTOPAQUE UNIVERSAL1994-09-08
K940306 — OCTOSTOP COMPENSATING FILTERS1994-09-06

Adverse events under product code KPR

product code KPR

Other: 6
Total: 6

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.