X-RAY POSITIONING DEVICE— 510(k) K770060

Name: FDA 510(k) clearance K770060
Creator: U.S. Food and Drug Administration
Published: 1977-01-24

Substantially Equivalent

Robert R. Moore

FDA 510(k) clearance K770060 for X-RAY POSITIONING DEVICE, Substantially Equivalent on 1977-01-24. Applicant: Robert R. Moore. Device class: 2.

Clearance details

Applicant: Robert R. Moore
Product code: Code KPR
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 1977-01-11
Decision date: 1977-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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More clearances from Robert R. Moore

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K770658 — EXERCISER, LEG, LOWER EXTREMITY1977-06-17
K770501 — KNEE CUFF FOR EXPRESSING FLUID1977-04-05
K770223 — HEAVY FOAM HEEL & ELBOW PROTECTORS1977-02-23
K770059 — ORTHOPEDIC SPECIALTIES1977-01-14

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.