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FDA 510(k)

STRYKER DROP APPLICATOR, KITS, SPRAY APPLICATOR KIT, TIPS

K-Number: K950824 · 1995-08-25

ApplicantStryker Corp.
Decision Date1995-08-25
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STRYKER DROP APPLICATOR, KITS, SPRAY APPLICATOR KIT, TIPS is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1995-08-25 under 510(k) number K950824. 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 STRYKER DROP APPLICATOR, KITS, SPRAY APPLICATOR KIT, TIPS?

STRYKER DROP APPLICATOR, KITS, SPRAY APPLICATOR KIT, TIPS is a medical device that received FDA 510(k) clearance on 1995-08-25. The listed applicant is Stryker Corp.. The 510(k) number is K950824.

When did STRYKER DROP APPLICATOR, KITS, SPRAY APPLICATOR KIT, TIPS receive FDA 510(k) clearance?

STRYKER DROP APPLICATOR, KITS, SPRAY APPLICATOR KIT, TIPS received FDA 510(k) clearance on 1995-08-25, under 510(k) number K950824.

Who is the listed applicant for STRYKER DROP APPLICATOR, KITS, SPRAY APPLICATOR KIT, TIPS?

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

What is the FDA product code for STRYKER DROP APPLICATOR, KITS, SPRAY APPLICATOR KIT, TIPS?

The FDA product code for STRYKER DROP APPLICATOR, KITS, SPRAY APPLICATOR KIT, TIPS is FMF.

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Other records listing Stryker Corp. as applicant

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Related Devices (Code: FMF)

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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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