ANGIOGRAPHY DRAPE PACK— 510(k) K902293

Unknown

Biocor Medical, Inc.

FDA 510(k) clearance K902293 for ANGIOGRAPHY DRAPE PACK, Unknown on 1990-07-19. Applicant: Biocor Medical, Inc..

Clearance details

Applicant: Biocor Medical, Inc.
Product code: Code LRO
Advisory panel: General, Plastic Surgery
Date received: 1990-05-22
Decision date: 1990-07-19
Decision: Unknown
Clearance type: Traditional
Location: Tyler, TX, 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.