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FDA 510(k)

3.5 MHZ CW DOPPLER PROBE MODEL NO. 8421802

K-Number: K852572 · 1985-09-19

Decision Date1985-09-19
Product CodeJAF
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

3.5 MHZ CW DOPPLER PROBE MODEL NO. 8421802 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1985-09-19 under 510(k) number K852572. The device is classified under product code JAF. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3.5 MHZ CW DOPPLER PROBE MODEL NO. 8421802?

3.5 MHZ CW DOPPLER PROBE MODEL NO. 8421802 is a medical device that received FDA 510(k) clearance on 1985-09-19. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K852572.

When did 3.5 MHZ CW DOPPLER PROBE MODEL NO. 8421802 receive FDA 510(k) clearance?

3.5 MHZ CW DOPPLER PROBE MODEL NO. 8421802 received FDA 510(k) clearance on 1985-09-19, under 510(k) number K852572.

Who is the listed applicant for 3.5 MHZ CW DOPPLER PROBE MODEL NO. 8421802?

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

What is the FDA product code for 3.5 MHZ CW DOPPLER PROBE MODEL NO. 8421802?

The FDA product code for 3.5 MHZ CW DOPPLER PROBE MODEL NO. 8421802 is JAF.

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 Siemens Medical Solutions USA, 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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Related Devices (Code: JAF)

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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