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FDA 510(k)

LEWIS SAFE SLEEVE

K-Number: K873960 · 1987-12-04

ApplicantCheri Lewis, D.D.S.
Decision Date1987-12-04
Product CodeEIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LEWIS SAFE SLEEVE is the device name listed in this FDA 510(k) record. The listed applicant is Cheri Lewis, D.D.S.. It received FDA 510(k) clearance on 1987-12-04 under 510(k) number K873960. The device is classified under product code EIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEWIS SAFE SLEEVE?

LEWIS SAFE SLEEVE is a medical device that received FDA 510(k) clearance on 1987-12-04. The listed applicant is Cheri Lewis, D.D.S.. The 510(k) number is K873960.

When did LEWIS SAFE SLEEVE receive FDA 510(k) clearance?

LEWIS SAFE SLEEVE received FDA 510(k) clearance on 1987-12-04, under 510(k) number K873960.

Who is the listed applicant for LEWIS SAFE SLEEVE?

The FDA 510(k) record lists Cheri Lewis, D.D.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LEWIS SAFE SLEEVE?

The FDA product code for LEWIS SAFE SLEEVE is EIF.

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Related Devices (Code: EIF)

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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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