COR­REC­TIONS & CLAR­I­FI­CA­TIONS

Modern Healthcare - - LATE NEWS -

A July 8 ar­ti­cle, “Repo­si­tion­ing re­pro­cess­ing” (p. 32), in­cor­rectly cited an FDA state­ment about in-house re­pro­cess­ing of re­us­able med­i­cal de­vices. It was not about third-party re­pro­cess­ing of sin­gle-use de­vices, the sub­ject of the ar­ti­cle. An FDA of­fi­cial said in 2006 that “avail­able data show that (sin­gle-use de­vices) can be re­pro­cessed with a rea­son­able as­sur­ance of safety and ef­fec­tive­ness.”

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