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Pulse® CR Aqua

INNOVATIVE HEALTHCARE CORPORATION · Model 194352 · UDI-DI 50813172023181

OPC LZC

510(k) clearances

Adverse events

Recalls

Facilities

Description

Gloves, Exam, Chloroprene, Non-Sterile, Powder-Free, Textured, Aqua, XL

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.