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FDA 510(k)

RF-1 CIRCUIT

K-Number: K871592 · 1987-05-22

ApplicantDiagnostic Imaging Specialists Corp.
Decision Date1987-05-22
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RF-1 CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Imaging Specialists Corp.. It received FDA 510(k) clearance on 1987-05-22 under 510(k) number K871592. The device is classified under product code IZH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RF-1 CIRCUIT?

RF-1 CIRCUIT is a medical device that received FDA 510(k) clearance on 1987-05-22. The listed applicant is Diagnostic Imaging Specialists Corp.. The 510(k) number is K871592.

When did RF-1 CIRCUIT receive FDA 510(k) clearance?

RF-1 CIRCUIT received FDA 510(k) clearance on 1987-05-22, under 510(k) number K871592.

Who is the listed applicant for RF-1 CIRCUIT?

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

What is the FDA product code for RF-1 CIRCUIT?

The FDA product code for RF-1 CIRCUIT is IZH.

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Other records listing Diagnostic Imaging Specialists Corp. 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.

K875106PB-A LEAD-ACID BATTERY CONVERSION KIT

Related Devices (Code: IZH)

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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