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FDA 510(k)

SLATER SLEEVE

K-Number: K926158 · 1993-03-19

ApplicantTadco, Inc.
Decision Date1993-03-19
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SLATER SLEEVE is the device name listed in this FDA 510(k) record. The listed applicant is Tadco, Inc.. It received FDA 510(k) clearance on 1993-03-19 under 510(k) number K926158. The device is classified under product code CCW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLATER SLEEVE?

SLATER SLEEVE is a medical device that received FDA 510(k) clearance on 1993-03-19. The listed applicant is Tadco, Inc.. The 510(k) number is K926158.

When did SLATER SLEEVE receive FDA 510(k) clearance?

SLATER SLEEVE received FDA 510(k) clearance on 1993-03-19, under 510(k) number K926158.

Who is the listed applicant for SLATER SLEEVE?

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

What is the FDA product code for SLATER SLEEVE?

The FDA product code for SLATER SLEEVE is CCW.

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.

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Other records listing Tadco, Inc. 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.

K905735GENNY DENNY IV SHIELD

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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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