GRAB BAR— 510(k) K780935

Name: FDA 510(k) clearance K780935
Creator: U.S. Food and Drug Administration
Published: 1978-06-19

Substantially Equivalent

Orthopedic Equipment Co., Inc.

FDA 510(k) clearance K780935 for GRAB BAR, Substantially Equivalent on 1978-06-19. Applicant: Orthopedic Equipment Co., Inc.. Device class: 1.

Clearance details

Applicant: Orthopedic Equipment Co., Inc.
Product code: Code IKX
Device class: Class 1
Regulation: 21 CFR 890.5050
Advisory panel: Physical Medicine
Date received: 1978-06-07
Decision date: 1978-06-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K831541 — TUB TRANSFER BENCH BK64811983-06-02
K823639 — BOARD TO TRANSFER PARALYZED PATIENT FROM1983-01-21
K823640 — BATH TUB SAFETY BAR1983-01-21

More clearances from Orthopedic Equipment Co., Inc.

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K834035 — UNIVERSAL SELF-ALIGNING ACETABULAR COM1984-06-19
K841189 — OEC/REZAIAN SPINAL FIXATOR1984-05-16
K800530 — SCHLEIN TRI-SURFACE ANKLE1980-04-02
K781445 — SPREADER1979-09-27
K790209 — FILTER SYSTEM, ALTNER DISPOSABLE1979-02-26

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.