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Spiracur, Inc.

Philadelphia, PA, US

Spiracur, Inc. appears in FDA device records in Philadelphia, PA. FDA records list 9 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
9
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 9 510(k) clearances for Spiracur, Inc. between 2009 and 2015. The busiest year on record is 2011, with 4. The most recent is 2015, with 1.

Clearances by year, as a table
510(k) clearance decisions for Spiracur, Inc., by decision year
YearClearances
20091
20114
20143
20151
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K151710SNaP Wound Care SystemOKOSubstantially Equivalent
K142272SNaP Wound Care SystemOKOSubstantially Equivalent
K132080SNAP WOUND CARE SYSTEMOKOSubstantially Equivalent
K133137CISNAP CLOSED INCISION SYSTEMOKOSubstantially Equivalent
K113032SNAP WOUND CARE SYSTEMOKOSubstantially Equivalent
K112341SNAP WOUND CARE SYSTEMOKOSubstantially Equivalent
K111393SNAP (R) WOUND CARE SYSTEMOKOSubstantially Equivalent
K111006CI-SNAP WOUND CARE SYSTEMOKOSubstantially Equivalent
DEN080011SNAP WOUND CARE DEVICEOKOUnknown

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain