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510(k) K780543

THERMAJUST CIRCU-TEMP by Techhnilab Instruments, Inc. — Product Code JRQ

K780543 is an FDA 510(k) premarket notification submitted by Techhnilab Instruments, Inc. for the device "THERMAJUST CIRCU-TEMP". The FDA issued a decision of Substantially Equivalent on May 26, 1978. The device falls under product code JRQ (Shaker/Stirrer), a Class I device regulated under 21 CFR 862.2050. Techhnilab Instruments, Inc. has at least 5 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 26, 1978
Date Received
April 3, 1978
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Shaker/Stirrer
Device Class
Class I
Regulation Number
862.2050
Review Panel
CH
Submission Type

Other clearances by Techhnilab Instruments, Inc.

  • K813523 — ELECTRIC SELF STERILIZATION INOCUL. LOOP (December 31, 1981)
  • K780544 — DISC-PAK ROTATOR (April 24, 1978)
  • K771434 — MULTI-CAVITY EQUILIBRIUM CELL (August 22, 1977)
  • K770169 — BEESON AUTOMADDAK FEEDER (January 28, 1977)
  • K770170 — MADDATHERM PARAFFIN BATH (January 28, 1977)

Other clearances for product code JRQ

  • K813318 — MINI-SHAKER (December 17, 1981)
  • K813148 — S/P VORTEX MIXER (November 24, 1981)
  • K813149 — S/P VORTEX MIXER JR. (November 24, 1981)
  • K801145 — SMI MULTI-TUBE VORTEXER (June 9, 1980)
  • K790753 — DIMENSIONALL ROTATOR (June 28, 1979)
  • K790027 — SHAKER, MODEL SH-510 (February 8, 1979)
  • K770165 — MICRO-MIX PIPETTE SHAKER (January 31, 1977)

FDA data resources