AIRVIEW BOWIE DICK; TEST PACK, INDICATOR SHEETS
K-Number: K130211 · 2013-07-05
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Device Summary
Frequently Asked Questions
What is the AIRVIEW BOWIE DICK; TEST PACK, INDICATOR SHEETS?
AIRVIEW BOWIE DICK; TEST PACK, INDICATOR SHEETS is a medical device that received FDA 510(k) clearance on 2013-07-05. The listed applicant is Spsmedical Supply Corp.. The 510(k) number is K130211.
When did AIRVIEW BOWIE DICK; TEST PACK, INDICATOR SHEETS receive FDA 510(k) clearance?
AIRVIEW BOWIE DICK; TEST PACK, INDICATOR SHEETS received FDA 510(k) clearance on 2013-07-05, under 510(k) number K130211.
Who is the listed applicant for AIRVIEW BOWIE DICK; TEST PACK, INDICATOR SHEETS?
The FDA 510(k) record lists Spsmedical Supply Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AIRVIEW BOWIE DICK; TEST PACK, INDICATOR SHEETS?
The FDA product code for AIRVIEW BOWIE DICK; TEST PACK, INDICATOR SHEETS is JOJ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Spsmedical Supply Corp. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: JOJ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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