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FDA 510(k)

APPLICATOR TIP/DUAL SPRAYER KIT

K-Number: K010708 · 2001-04-30

ApplicantInterpore Cross Intl.
Decision Date2001-04-30
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

APPLICATOR TIP/DUAL SPRAYER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Interpore Cross Intl.. It received FDA 510(k) clearance on 2001-04-30 under 510(k) number K010708. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APPLICATOR TIP/DUAL SPRAYER KIT?

APPLICATOR TIP/DUAL SPRAYER KIT is a medical device that received FDA 510(k) clearance on 2001-04-30. The listed applicant is Interpore Cross Intl.. The 510(k) number is K010708.

When did APPLICATOR TIP/DUAL SPRAYER KIT receive FDA 510(k) clearance?

APPLICATOR TIP/DUAL SPRAYER KIT received FDA 510(k) clearance on 2001-04-30, under 510(k) number K010708.

Who is the listed applicant for APPLICATOR TIP/DUAL SPRAYER KIT?

The FDA 510(k) record lists Interpore Cross Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for APPLICATOR TIP/DUAL SPRAYER KIT?

The FDA product code for APPLICATOR TIP/DUAL SPRAYER KIT is FMF.

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Other records listing Interpore Cross Intl. as applicant

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Related Devices (Code: FMF)

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

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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