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FDA 510(k)

PRESATURATION

K-Number: K920835 · 1992-05-22

ApplicantResonex, Inc.
Decision Date1992-05-22
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PRESATURATION is the device name listed in this FDA 510(k) record. The listed applicant is Resonex, Inc.. It received FDA 510(k) clearance on 1992-05-22 under 510(k) number K920835. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESATURATION?

PRESATURATION is a medical device that received FDA 510(k) clearance on 1992-05-22. The listed applicant is Resonex, Inc.. The 510(k) number is K920835.

When did PRESATURATION receive FDA 510(k) clearance?

PRESATURATION received FDA 510(k) clearance on 1992-05-22, under 510(k) number K920835.

Who is the listed applicant for PRESATURATION?

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

What is the FDA product code for PRESATURATION?

The FDA product code for PRESATURATION is LNH.

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Other records listing Resonex, Inc. as applicant

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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