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FDA 510(k)

RTS TECHNOLOGY MODELS 721,722,723,724

K-Number: K914578 · 1992-02-28

ApplicantRts Technology, Inc.
Decision Date1992-02-28
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RTS TECHNOLOGY MODELS 721,722,723,724 is the device name listed in this FDA 510(k) record. The listed applicant is Rts Technology, Inc.. It received FDA 510(k) clearance on 1992-02-28 under 510(k) number K914578. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RTS TECHNOLOGY MODELS 721,722,723,724?

RTS TECHNOLOGY MODELS 721,722,723,724 is a medical device that received FDA 510(k) clearance on 1992-02-28. The listed applicant is Rts Technology, Inc.. The 510(k) number is K914578.

When did RTS TECHNOLOGY MODELS 721,722,723,724 receive FDA 510(k) clearance?

RTS TECHNOLOGY MODELS 721,722,723,724 received FDA 510(k) clearance on 1992-02-28, under 510(k) number K914578.

Who is the listed applicant for RTS TECHNOLOGY MODELS 721,722,723,724?

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

What is the FDA product code for RTS TECHNOLOGY MODELS 721,722,723,724?

The FDA product code for RTS TECHNOLOGY MODELS 721,722,723,724 is JAQ.

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Other records listing Rts Technology, 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.

K912555GAMMAMED 12IT HIGH DOSE RATE REMOTE AFTERLOADERK901589RTS TECHNOLOGY IRIDIUM 192 SOURCES

Related Devices (Code: JAQ)

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.

K262383LumenCare AzureNucletron B.V.K252717MAASTRO Rectal Applicator SetVarian Medical SystemsK251037Rectal ApplicatorNucletron B.V.K252884Guided Aarhus Applicator SetVarian Medical SystemsK250299CT/ MR Tandem and Ovoid SetVarian Medical Systems, Inc.K250289Intracavitary/Interstitial SystemVarian Medical Systems

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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