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510(k) K871408

BLOOD VESSEL CONNECTOR by Quali-Med, Inc.

K871408 is an FDA 510(k) premarket notification submitted by Quali-Med, Inc. for the device "BLOOD VESSEL CONNECTOR". The FDA issued a decision of Substantially Equivalent on Apr 27, 1987. Quali-Med, Inc. has 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Apr 27, 1987
Date Received
Apr 8, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Quali-Med, Inc.

  • K862972 — DISPOSABLE MIRROR (Sep 23, 1986)
  • K862472 — QUARTZ RODS TITANIUM RODS (Sep 12, 1986)
  • K862241 — STANDARD BASIN KIT CUSTOM BASIN KIT (Aug 1, 1986)
  • K862242 — PAP SMEAR KIT (Jun 26, 1986)
  • K862172 — QUALI-MED'S OPERATING ROOM DRAPES (Jun 19, 1986)
  • K861198 — CUSTOM PROCEDURE KIT (VARIOUS SUB-TITLES) (May 16, 1986)

FDA data resources