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510(k) K791970

HYGENIC RUBBER DAM LUBRICANT by The Hygenic Corp. — Product Code KMJ

K791970 is an FDA 510(k) premarket notification submitted by The Hygenic Corp. for the device "HYGENIC RUBBER DAM LUBRICANT". The FDA issued a decision of Substantially Equivalent on November 16, 1979. The device falls under product code KMJ (Lubricant, Patient), a Class I device regulated under 21 CFR 880.6375. The Hygenic Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 16, 1979
Date Received
October 2, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Lubricant, Patient
Device Class
Class I
Regulation Number
880.6375
Review Panel
HO
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 KMJ

  • K142473 — Lubricating Jelly (April 13, 2015)
  • K141028 — COLONGLIDE LUBRICANT (July 24, 2014)
  • K131617 — COLONGLIDE(R) LUBRICANT (October 3, 2013)
  • K121390 — LUBE JELLY SURINGE (August 10, 2012)
  • K113689 — DUKAL LUBRICATING JELLY (May 4, 2012)
  • K112110 — STERILE LUBRICATING JELLY (April 10, 2012)
  • K103718 — DYNACOR LUBRICATION GEL (May 10, 2011)
  • K101522 — ULTRA SEAL STERILE LUBRICATING JELLY (December 23, 2010)
  • K092488 — DYNAREX STERILE LUBRICATING JELLY (December 18, 2009)
  • K083189 — STERI-LUB LUBRICATION GEL (November 21, 2008)

FDA data resources