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510(k) K850863

ULTRAFIL-LT (GUTTA PERCHA) by The Hygenic Corp. — Product Code EKM

K850863 is an FDA 510(k) premarket notification submitted by The Hygenic Corp. for the device "ULTRAFIL-LT (GUTTA PERCHA)". The FDA issued a decision of Substantially Equivalent on April 16, 1985. The device falls under product code EKM (Gutta-Percha), a Class I device regulated under 21 CFR 872.3850. The Hygenic Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 16, 1985
Date Received
March 1, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Gutta-Percha
Device Class
Class I
Regulation Number
872.3850
Review Panel
DE
Submission Type

Other clearances by The Hygenic Corp.

  • K954990 — DENTAL DAM (January 26, 1996)
  • K930764 — ENDO-ICE-PULP TESTER-THERMAL (May 27, 1993)
  • K905418 — GATES GLIDDEN DRILLS (July 25, 1991)
  • K911225 — TRAY DOUGH (April 17, 1991)
  • K905640 — SOLID CORE GUTTA PERCHA CARRIER (March 5, 1991)
  • K900301 — NOVUS BONDING AGENT (May 15, 1990)
  • K900844 — WEDJETS (April 16, 1990)
  • K894092 — DENTAL ENDODONTIC CEMENT (MODIFICATION) (January 10, 1990)
  • K881826 — ENDO-ICE (August 23, 1988)
  • K873644 — PULP PEN (October 27, 1987)

Other clearances for product code EKM

  • K073369 — EI DOWNPAK BARRIER SLEEVES (February 27, 2008)
  • K070246 — DOWN PAK (February 16, 2007)
  • K051573 — TGP (GUTTA PERCHA CONTAINING TETRACYCLINE OR DOXYCYCLINE) (June 26, 2006)
  • K042870 — ENDO TWINN (January 11, 2005)
  • K023819 — FIBERFILL SGP (March 26, 2003)
  • K971641 — ANTIBACTERIAL GUTTA PERCHA (July 21, 1997)
  • K970134 — THERMAPREP PLUS OVEN (March 21, 1997)
  • K931742 — INJECT-R FILL (May 27, 1993)
  • K924825 — MICRODOSE RC-EZ (March 5, 1993)
  • K915243 — TOUCH 'N HEAT MODEL 5002, MODIFICATION (January 21, 1992)

FDA data resources