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510(k) K790753

DIMENSIONALL ROTATOR by American Hospital Supply Corp. — Product Code JRQ

K790753 is an FDA 510(k) premarket notification submitted by American Hospital Supply Corp. for the device "DIMENSIONALL ROTATOR". The FDA issued a decision of Substantially Equivalent on June 28, 1979. The device falls under product code JRQ (Shaker/Stirrer), a Class I device regulated under 21 CFR 862.2050. American Hospital Supply Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 28, 1979
Date Received
April 17, 1979
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 American Hospital Supply Corp.

  • K854739 — AMERICAN STERILE SURGICAL ABSORBENT TOWEL (December 27, 1985)
  • K854759 — AMERICAN STERILE MAYO STAND TRAY (December 17, 1985)
  • K832826 — AAP DOSIMETRY RELEASE OR BASIN SETS (April 23, 1984)
  • K830546 — DOSIMETRIC RELEASE (May 25, 1983)
  • K822990 — CONVERTORS PRIMARY WOUND DRESSING II (April 12, 1983)
  • K830343 — CONTAINER W/PRIMING SOLUTION (March 17, 1983)
  • K830301 — STRATUS FLUOROMETRIC ENZYME IMMUN0- (February 25, 1983)
  • K822755 — LATEX PENROSE TUBING (January 21, 1983)
  • K823418 — HEYER-SCHUTE UNIVERSAL URETERAL STENT (December 3, 1982)
  • K822966 — CONVERTORS DISPOSABLE DRESSING SPONGE (November 5, 1982)

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)
  • K790027 — SHAKER, MODEL SH-510 (February 8, 1979)
  • K780543 — THERMAJUST CIRCU-TEMP (May 26, 1978)
  • K770165 — MICRO-MIX PIPETTE SHAKER (January 31, 1977)

FDA data resources