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FDA 510(k)

PANA-SPRAY

K-Number: K052700 · 2005-12-20

Decision Date2005-12-20
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PANA-SPRAY is the device name listed in this FDA 510(k) record. The listed applicant is Nsk America Corp.. It received FDA 510(k) clearance on 2005-12-20 under 510(k) number K052700. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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