Atlas FDA

SMARTSPONGE SYSTEM

FDA 510(k) clearance K071355 · decided 2007-05-24

Clearance details

K-number
K071355
Device name
SMARTSPONGE SYSTEM
Applicant
Clearcount Medical Solutions, Inc.
Decision
Substantially Equivalent
Date received
2007-05-15
Decision date
2007-05-24
Days to decision
9 days
Clearance type
Traditional
Product code
LWH
Device class
1
Regulation number
880.2740
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Pittsburgh, PA, US
Third-party review
Yes
Expedited review
No

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RecordFirmDate
PIXEL APP (K121274)Gauss Surgical, Inc.,2012-06-27
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ORLOCATE SYSTEM MODEL ORL 100 (K100551)Haldor Advanced Technologies, Ltd.2010-08-12
SMARTWAND-DTX (K093557)Clearcount Medical Solutions2009-12-18
SMARTSPONGE PLUS SYSTEM (K073180)Clearcount Medical Solutions, Inc.2007-11-19
RF SURGICAL SYSTEMS INC. DETECTION SYSTEM, MODEL 100A (K062642)Rf Surgical Systems, Inc.2006-11-02
MEDLINE SURGICAL SPONGE SCANNER (K061316)Medline Industries, Inc.2006-11-02
SURGICOUNT SAFETY-SPONGE SYSTEM (K060076)Surgicount Medical2006-03-14
MARKWELL GAUZE SPONGE (K982260)Markwell Intl., Inc.1998-08-12
POCKET COUNT OR SAFETCOUNT (K972302)Sage Products, Inc.1997-07-25
SPONGE COUNT (K945144)Michael Fischer Assoc.1995-01-12
DEVON SPONGE COUNTER BAGS (K912824)Devon Industries, Inc.1991-08-26

Recalls involving this device

No recalls on record reference this clearance.