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FDA 510(k)

OSSPRAY CLEANING COMPOUND

K-Number: K062502 · 2006-12-15

ApplicantOspray, Ltd.
Decision Date2006-12-15
Product CodeEJR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

OSSPRAY CLEANING COMPOUND is the device name listed in this FDA 510(k) record. The listed applicant is Ospray, Ltd.. It received FDA 510(k) clearance on 2006-12-15 under 510(k) number K062502. The device is classified under product code EJR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSSPRAY CLEANING COMPOUND?

OSSPRAY CLEANING COMPOUND is a medical device that received FDA 510(k) clearance on 2006-12-15. The listed applicant is Ospray, Ltd.. The 510(k) number is K062502.

When did OSSPRAY CLEANING COMPOUND receive FDA 510(k) clearance?

OSSPRAY CLEANING COMPOUND received FDA 510(k) clearance on 2006-12-15, under 510(k) number K062502.

Who is the listed applicant for OSSPRAY CLEANING COMPOUND?

The FDA 510(k) record lists Ospray, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OSSPRAY CLEANING COMPOUND?

The FDA product code for OSSPRAY CLEANING COMPOUND is EJR.

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Related Devices (Code: EJR)

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.

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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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