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FDA 510(k)

TDP, LARK BRAND AND MIT LAMP

K-Number: K875052 · 1988-06-23

ApplicantI.E.C. Co.
Decision Date1988-06-23
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TDP, LARK BRAND AND MIT LAMP is the device name listed in this FDA 510(k) record. The listed applicant is I.E.C. Co.. It received FDA 510(k) clearance on 1988-06-23 under 510(k) number K875052. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TDP, LARK BRAND AND MIT LAMP?

TDP, LARK BRAND AND MIT LAMP is a medical device that received FDA 510(k) clearance on 1988-06-23. The listed applicant is I.E.C. Co.. The 510(k) number is K875052.

When did TDP, LARK BRAND AND MIT LAMP receive FDA 510(k) clearance?

TDP, LARK BRAND AND MIT LAMP received FDA 510(k) clearance on 1988-06-23, under 510(k) number K875052.

Who is the listed applicant for TDP, LARK BRAND AND MIT LAMP?

The FDA 510(k) record lists I.E.C. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TDP, LARK BRAND AND MIT LAMP?

The FDA product code for TDP, LARK BRAND AND MIT LAMP is ILY.

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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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