
Procter & Gamble Mfg. Co.
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BOUNDARY SINGLE-USE GOWNS is an FDA 510(k)-cleared medical device (K841255) manufactured by Procter & Gamble Mfg. Co.. This device is classified under the Unknown specialty. FDA clearance granted on April 24, 1984.

Ansell
SKU MSC846624

Princeton BioMeditech Corp.
SKU K014192

McKesson
SKU VM-1270030

Hollister
SKU VM-1270031