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510(k) K851386

UNITEK DISPOSABLE IMPRESSION SYRINGE by Unitek Corp. — Product Code EID

K851386 is an FDA 510(k) premarket notification submitted by Unitek Corp. for the device "UNITEK DISPOSABLE IMPRESSION SYRINGE". The FDA issued a decision of Substantially Equivalent on April 29, 1985. The device falls under product code EID (Syringe, Restorative And Impression Material), a Class I device regulated under 21 CFR 872.4565. Unitek Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 29, 1985
Date Received
April 9, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Syringe, Restorative And Impression Material
Device Class
Class I
Regulation Number
872.4565
Review Panel
DE
Submission Type

Other clearances by Unitek Corp.

  • K944286 — METAL-LINED TRANSCEND CERAMIC BRACKET (November 29, 1994)
  • K933501 — ALASTIK (April 28, 1994)
  • K940165 — ALASTIK (March 7, 1994)
  • K923999 — ALASTIK NS (June 24, 1993)
  • K924645 — TRANSCEND SERIES 6000 DEBONDING INSTRUMENTS (November 25, 1992)
  • K924295 — DEBRACKETING INSTRUMENT (November 23, 1992)
  • K923432 — GERMAN MINI DYNALOCK (October 30, 1992)
  • K911271 — ADHESIVE PRECOATED BRACKETS (May 29, 1991)
  • K910288 — NONSTAINING ALASTIKS (March 29, 1991)
  • K890529 — ALASTIGARD (March 9, 1989)

Other clearances for product code EID

  • K941431 — BONE GRAFT DELIVERY SYRINGES (July 12, 1994)
  • K913974 — ACCESS IMPRESSION BARREL (February 25, 1992)
  • K873153 — CAULK'S VPS CARTRIDGE SYSTEM (September 16, 1987)
  • K871937 — IMPRESSION SYRINGE (June 5, 1987)
  • K863998 — COLTENE JET-MIXER (October 30, 1986)
  • K853282 — CENTRIX RIBBON TUBES (August 23, 1985)
  • K812680 — G-C IMPRESSION SYRINGE (October 6, 1981)
  • K812277 — PRISMA-FIL COMPULES (September 8, 1981)
  • K811582 — THE PLACER (July 28, 1981)
  • K781977 — APPLICATOR, LEE IMPRESSION (December 20, 1978)

FDA data resources