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FDA 510(k)

STERISTORAGE CONTAINER

K-Number: K853450 · 1986-03-18

ApplicantK-Seven Industries, Inc.
Decision Date1986-03-18
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERISTORAGE CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is K-Seven Industries, Inc.. It received FDA 510(k) clearance on 1986-03-18 under 510(k) number K853450. 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 STERISTORAGE CONTAINER?

STERISTORAGE CONTAINER is a medical device that received FDA 510(k) clearance on 1986-03-18. The listed applicant is K-Seven Industries, Inc.. The 510(k) number is K853450.

When did STERISTORAGE CONTAINER receive FDA 510(k) clearance?

STERISTORAGE CONTAINER received FDA 510(k) clearance on 1986-03-18, under 510(k) number K853450.

Who is the listed applicant for STERISTORAGE CONTAINER?

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

What is the FDA product code for STERISTORAGE CONTAINER?

The FDA product code for STERISTORAGE CONTAINER is FMF.

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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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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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