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510(k) K854900

EPISIOTOMY SCISSORS by Euro-Med Intl.

K854900 is an FDA 510(k) premarket notification submitted by Euro-Med Intl. for the device "EPISIOTOMY SCISSORS". The FDA issued a decision of Substantially Equivalent on Dec 24, 1985. Euro-Med Intl. has 15 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Dec 24, 1985
Date Received
Dec 6, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Euro-Med Intl.

  • K883884 — PROSTATIC CORE-CUT NEEDLE (Dec 5, 1988)
  • K882404 — KEVOR-CURETTE (Jul 8, 1988)
  • K854901 — PACIFIC GRASPER (May 2, 1986)
  • K854898 — ATLANTIC GRASPER (May 2, 1986)
  • K854896 — HOOK SCISSOR (May 2, 1986)
  • K854894 — SPOON (May 2, 1986)
  • K854890 — HOOK PROBE (May 2, 1986)
  • K854895 — BASKET FORCEP (May 2, 1986)
  • K854891 — KNIFE (May 2, 1986)
  • K854897 — MAX-I-GRASP (May 2, 1986)

FDA data resources