FDA applicant

Harry A. Schlakman

Elizabeth, NJ2 decisions1995–19950 recalls

FDA records 2 decisions for Harry A. Schlakman (Elizabeth, NJ) in 1995: 2 510(k) clearances. Most are in product codes KDW (Container, Specimen Mailer And Storage…) and KOB (Catheter, Suprapubic (And Accessories)). 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, pathology panel, where it files most

How often FDA has decided Harry A. Schlakman’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Harry A. Schlakman since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Harry A. Schlakman by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Harry”

FDA records each applicant name separately; these may or may not be the same firm.

Harry J. Bosworth Co. 45 Harry Panzer Intl. Corp. 2

Harry A. Schlakman

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Harry”