Atlas FDA

SPSMEDICAL SPORVIEW PA CULTURE SET

FDA 510(k) clearance K081879 · decided 2008-07-30

Clearance details

K-number
K081879
Device name
SPSMEDICAL SPORVIEW PA CULTURE SET
Applicant
Spsmedical Supply Corp.
Decision
Substantially Equivalent
Date received
2008-07-02
Decision date
2008-07-30
Days to decision
28 days
Clearance type
Special
Product code
MRB
Device class
2
Regulation number
880.2800
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Rush, NY, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
RAVEN PROPACT (K053212)Raven Biological Laboratories, Inc.2006-02-15
SPSMEDICAL SPORVIEW PA CULTURE SET (K043135)Spsmedical Supply Corp.2005-01-13
PRO-PACT PERACETIC ACID CULTURE TEST KIT, MODEL C-3PA (K031114)Raven Biological Laboratories, Inc.2004-03-03

Recalls involving this device

No recalls on record reference this clearance.