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510(k) K862335

MODIFIED I.V. START, RE-START, PEDI AND GERI-KIT by U.S. Mfg. & Management, Inc.

K862335 is an FDA 510(k) premarket notification submitted by U.S. Mfg. & Management, Inc. for the device "MODIFIED I.V. START, RE-START, PEDI AND GERI-KIT". The FDA issued a decision of SN on July 24, 1986. U.S. Mfg. & Management, Inc. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
July 24, 1986
Date Received
June 19, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by U.S. Mfg. & Management, Inc.

  • K920860 — CONTROLLED PASSIVE MOTION MACHINE (April 2, 1992)
  • K874436 — FLUID SAMPLING PACK (January 5, 1988)
  • K853242 — I.V. START KIT, I.V. RESTART KIT, PEDI-KIT,GERI-KI (August 30, 1985)
  • K842999 — VENI-SHIELD (September 24, 1984)

FDA data resources