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FDA 510(k)

CUSTOM STERILE PROCEDURE TRAYS-MULTI

K-Number: K841850 · 1984-08-24

ApplicantSterilco, Inc.
Decision Date1984-08-24
Product Code
DecisionSubstantially Equivalent

Device Summary

CUSTOM STERILE PROCEDURE TRAYS-MULTI is the device name listed in this FDA 510(k) record. The listed applicant is Sterilco, Inc.. It received FDA 510(k) clearance on 1984-08-24 under 510(k) number K841850. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUSTOM STERILE PROCEDURE TRAYS-MULTI?

CUSTOM STERILE PROCEDURE TRAYS-MULTI is a medical device that received FDA 510(k) clearance on 1984-08-24. The listed applicant is Sterilco, Inc.. The 510(k) number is K841850.

When did CUSTOM STERILE PROCEDURE TRAYS-MULTI receive FDA 510(k) clearance?

CUSTOM STERILE PROCEDURE TRAYS-MULTI received FDA 510(k) clearance on 1984-08-24, under 510(k) number K841850.

Who is the listed applicant for CUSTOM STERILE PROCEDURE TRAYS-MULTI?

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

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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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