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FDA 510(k)

MODEL 499 SSR ANALYSIS SYSTEM

K-Number: K884887 · 1989-02-06

Decision Date1989-02-06
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 499 SSR ANALYSIS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Del Mar Avionics. It received FDA 510(k) clearance on 1989-02-06 under 510(k) number K884887. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 499 SSR ANALYSIS SYSTEM?

MODEL 499 SSR ANALYSIS SYSTEM is a medical device that received FDA 510(k) clearance on 1989-02-06. The listed applicant is Del Mar Avionics. The 510(k) number is K884887.

When did MODEL 499 SSR ANALYSIS SYSTEM receive FDA 510(k) clearance?

MODEL 499 SSR ANALYSIS SYSTEM received FDA 510(k) clearance on 1989-02-06, under 510(k) number K884887.

Who is the listed applicant for MODEL 499 SSR ANALYSIS SYSTEM?

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

What is the FDA product code for MODEL 499 SSR ANALYSIS SYSTEM?

The FDA product code for MODEL 499 SSR ANALYSIS SYSTEM is DSI.

Related Clinical Trials

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.

Other records listing Del Mar Avionics 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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Related Devices (Code: DSI)

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.

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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