DeviceClearance

MODIFIED I.V. START, RE-START, PEDI AND GERI-KIT— 510(k) K862335

Substantially Equivalent for Some Indications

U.S. Mfg. & Management, Inc.

FDA 510(k) clearance K862335 for MODIFIED I.V. START, RE-START, PEDI AND GERI-KIT, Substantially Equivalent for Some Indications on 1986-07-24. Applicant: U.S. Mfg. & Management, Inc..

Clearance details

Applicant
U.S. Mfg. & Management, Inc.
Advisory panel
Unknown
Date received
Decision date
Decision
Substantially Equivalent for Some Indications
Clearance type
Traditional
Location
San Bernardino, CA, US
Download summary PDFView on FDA.gov ↗

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