MEDLINES REPEAT PERFORMANCE SURGICAL PACK SYSTEM— 510(k) K930700

Unknown

Medline Industries, Inc.

FDA 510(k) clearance K930700 for MEDLINES REPEAT PERFORMANCE SURGICAL PACK SYSTEM, Unknown on 1993-07-09. Applicant: Medline Industries, Inc..

Clearance details

Applicant: Medline Industries, Inc.
Product code: Code LRO
Advisory panel: General, Plastic Surgery
Date received: 1993-02-10
Decision date: 1993-07-09
Decision: Unknown
Clearance type: Traditional
Location: Mundelein, IL, US

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Adverse events under product code LRO

product code LRO

Injury: 975
Malfunction: 14,038
Other: 2
Total: 15,015

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.