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FDA 510(k)

SECUTAINER

K-Number: K902709 · 1990-07-27

ApplicantPreserve
Decision Date1990-07-27
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SECUTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Preserve. It received FDA 510(k) clearance on 1990-07-27 under 510(k) number K902709. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SECUTAINER?

SECUTAINER is a medical device that received FDA 510(k) clearance on 1990-07-27. The listed applicant is Preserve. The 510(k) number is K902709.

When did SECUTAINER receive FDA 510(k) clearance?

SECUTAINER received FDA 510(k) clearance on 1990-07-27, under 510(k) number K902709.

Who is the listed applicant for SECUTAINER?

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

What is the FDA product code for SECUTAINER?

The FDA product code for SECUTAINER is JKA.

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Related Devices (Code: JKA)

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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