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510(k) K073180

SMARTSPONGE PLUS SYSTEM by Clearcount Medical Solutions, Inc. — Product Code LWH

K073180 is an FDA 510(k) premarket notification submitted by Clearcount Medical Solutions, Inc. for the device "SMARTSPONGE PLUS SYSTEM". The FDA issued a decision of Substantially Equivalent on November 19, 2007. The device falls under product code LWH (Counter, Sponge, Surgical), a Class I device regulated under 21 CFR 880.2740. Clearcount Medical Solutions, Inc. has at least 2 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 19, 2007
Date Received
November 13, 2007
Clearance Type
Traditional
Expedited Review
No
Third Party Review
Yes

Device Classification

Device Name
Counter, Sponge, Surgical
Device Class
Class I
Regulation Number
880.2740
Review Panel
SU
Submission Type

Other clearances by Clearcount Medical Solutions, Inc.

  • K093557 — SMARTWAND-DTX (December 18, 2009)
  • K071355 — SMARTSPONGE SYSTEM (May 24, 2007)

Other clearances for product code LWH

  • K121274 — PIXEL APP (June 27, 2012)
  • K120473 — PIXEL APP (April 9, 2012)
  • K100551 — ORLOCATE SYSTEM MODEL ORL 100 (August 12, 2010)
  • K093557 — SMARTWAND-DTX (December 18, 2009)
  • K071355 — SMARTSPONGE SYSTEM (May 24, 2007)
  • K061316 — MEDLINE SURGICAL SPONGE SCANNER (November 2, 2006)
  • K062642 — RF SURGICAL SYSTEMS INC. DETECTION SYSTEM, MODEL 100A (November 2, 2006)
  • K060076 — SURGICOUNT SAFETY-SPONGE SYSTEM (March 14, 2006)
  • K982260 — MARKWELL GAUZE SPONGE (August 12, 1998)
  • K972302 — POCKET COUNT OR SAFETCOUNT (July 25, 1997)

FDA data resources