LEUKOCLIP(R)— 510(k) K873744

Substantially Equivalent

Beiersdorf, Inc.

FDA 510(k) clearance K873744 for LEUKOCLIP(R), Substantially Equivalent on 1987-09-30. Applicant: Beiersdorf, Inc.. Device class: 1.

Clearance details

Applicant: Beiersdorf, Inc.
Product code: Code FZQ
Device class: Class 1
Regulation: 21 CFR 878.4320
Advisory panel: General, Plastic Surgery
Date received: 1987-09-16
Decision date: 1987-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwalk, CT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FZQ

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K830768 — DISPOSABLE SKIN STAPLER1983-04-12
K822963 — SURGICAL PRODUCTS, SKIN STAPLE REMOVER1982-11-08
K822145 — COMPLETE1982-10-22

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K952526 — CUTINOVA CAVITY1995-08-14
K943363 — CUTIPLAST STERIL1995-03-15
K944581 — CUTINOVA THIN WOUND DRESSING1994-12-02

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