PANA-SPRAY
K-Number: K052700 · 2005-12-20
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Device Summary
Frequently Asked Questions
What is the PANA-SPRAY?
PANA-SPRAY is a medical device that received FDA 510(k) clearance on 2005-12-20. The listed applicant is Nsk America Corp.. The 510(k) number is K052700.
When did PANA-SPRAY receive FDA 510(k) clearance?
PANA-SPRAY received FDA 510(k) clearance on 2005-12-20, under 510(k) number K052700.
Who is the listed applicant for PANA-SPRAY?
The FDA 510(k) record lists Nsk America Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PANA-SPRAY?
The FDA product code for PANA-SPRAY is EFB.
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 Nsk America 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: EFB)
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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