SLIDING BOARD— 510(k) K772417

Name: FDA 510(k) clearance K772417
Creator: U.S. Food and Drug Administration
Published: 1978-01-05

Substantially Equivalent

Fred Sammons, Inc.

FDA 510(k) clearance K772417 for SLIDING BOARD, Substantially Equivalent on 1978-01-05. Applicant: Fred Sammons, Inc.. Device class: 1.

Clearance details

Applicant: Fred Sammons, Inc.
Product code: Code IKX
Device class: Class 1
Regulation: 21 CFR 890.5050
Advisory panel: Physical Medicine
Date received: 1977-12-27
Decision date: 1978-01-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K823639 — BOARD TO TRANSFER PARALYZED PATIENT FROM1983-01-21
K823640 — BATH TUB SAFETY BAR1983-01-21

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K831549 — ARM SLINGS1983-06-30
K831548 — SPLINTS1983-06-27
K831542 — ADJUSTABLE POLYCENTRIC ELBOW HINGE1983-06-24

Adverse events under product code IKX

product code IKX

Death: 11
Total: 11

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.