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510(k) K830625

CYTO-STAIN by Richard-Allan Medical Ind., Inc. — Product Code HJQ

K830625 is an FDA 510(k) premarket notification submitted by Richard-Allan Medical Ind., Inc. for the device "CYTO-STAIN". The FDA issued a decision of Substantially Equivalent on March 24, 1983. The device falls under product code HJQ (Stereoscope, Ac-Powered), a Class I device regulated under 21 CFR 886.1870. Richard-Allan Medical Ind., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 24, 1983
Date Received
March 1, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stereoscope, Ac-Powered
Device Class
Class I
Regulation Number
886.1870
Review Panel
OP
Submission Type

Other clearances by Richard-Allan Medical Ind., Inc.

  • K931879 — REFLEX HTR (March 24, 1994)
  • K924200 — REFLEX(R) ESC (February 22, 1994)
  • K926297 — REFLEX ESI (October 15, 1993)
  • K924761 — STERILE ENDOSCOPIC DISPOS TROCARS W/SAFE SHIELD (April 20, 1993)
  • K900566 — RICHARD-ALLAN VESSEL LOOPS (May 3, 1990)
  • K896262 — TITANIUM LIGATING CLIPS (January 2, 1990)
  • K890314 — PROTECTOR (SURGICAL INSTRUMENT) (February 27, 1989)
  • K873309 — REFLEX(TM) CA-T CLIP APPLIER (November 27, 1987)
  • K862404 — REFLEX(TM) CLIP APPLIER (July 23, 1986)
  • K862223 — MICRO THIN* PARAFFIN (June 17, 1986)

FDA data resources