510(k) Report

FDA applicant

In Wha Pharmaceutical Co., Ltd.

Korea, KR1 decision1991–19910 recalls

FDA records 1 decision for In Wha Pharmaceutical Co., Ltd. (Korea, KR) in 1991: 1 510(k) clearance. All are in product code JII (Atomic Absorption, Lithium). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, clinical toxicology panel, where it files most

How often FDA has decided In Wha Pharmaceutical Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for In Wha Pharmaceutical Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — In Wha Pharmaceutical Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like In Wha Pharmaceutical Co., Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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