LIGACLIP 20/20* MULTIPLE CLIP APPLIER— 510(k) K864102

Substantially Equivalent

ETHICON, Inc.

FDA 510(k) clearance K864102 for LIGACLIP 20/20* MULTIPLE CLIP APPLIER, Substantially Equivalent on 1986-11-05. Applicant: ETHICON, Inc.. Device class: 2.

Clearance details

Applicant
ETHICON, Inc.
Product code
Code FZP
Device class
Class 2
Regulation
21 CFR 878.4300
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Somerville, NJ, US
Download summary PDFView on FDA.gov ↗

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More clearances from ETHICON, Inc.

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Adverse events under product code FZP

product code FZP
Death
11
Injury
726
Malfunction
10,830
Other
1
Total
11,568

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K864102

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K864102.

Data sourced from openFDA. This site is unofficial and independent of the FDA.