E-Z HOLD - #4060— 510(k) K864190

Name: FDA 510(k) clearance K864190
Creator: U.S. Food and Drug Administration
Published: 1987-01-14

Substantially Equivalent

John F. Greer Co., Inc.

FDA 510(k) clearance K864190 for E-Z HOLD - #4060, Substantially Equivalent on 1987-01-14. Applicant: John F. Greer Co., Inc.. Device class: 1.

Clearance details

Applicant: John F. Greer Co., Inc.
Product code: Code KMK
Device class: Class 1
Regulation: 21 CFR 880.5210
Advisory panel: General Hospital
Date received: 1986-10-27
Decision date: 1987-01-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oakland, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from John F. Greer Co., Inc.

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K870577 — E-Z LOOP1987-04-17
K870531 — EZ TAC FILTER1987-04-10
K864188 — E-Z HOLD WITH ADHESIVE BASE.-#40651986-12-04
K864189 — ULTRA-GEL - #40831986-12-04

Adverse events under product code KMK

product code KMK

Malfunction: 461
Other: 1
Total: 462

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.