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FDA 510(k)

EMS SWISS LITHOCLAST LITHOTRIPTER

K-Number: K963285 · 1997-02-13

Decision Date1997-02-13
Product CodeFFK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EMS SWISS LITHOCLAST LITHOTRIPTER is the device name listed in this FDA 510(k) record. The listed applicant is Electro Medical Systems SA. It received FDA 510(k) clearance on 1997-02-13 under 510(k) number K963285. The device is classified under product code FFK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMS SWISS LITHOCLAST LITHOTRIPTER?

EMS SWISS LITHOCLAST LITHOTRIPTER is a medical device that received FDA 510(k) clearance on 1997-02-13. The listed applicant is Electro Medical Systems SA. The 510(k) number is K963285.

When did EMS SWISS LITHOCLAST LITHOTRIPTER receive FDA 510(k) clearance?

EMS SWISS LITHOCLAST LITHOTRIPTER received FDA 510(k) clearance on 1997-02-13, under 510(k) number K963285.

Who is the listed applicant for EMS SWISS LITHOCLAST LITHOTRIPTER?

The FDA 510(k) record lists Electro Medical Systems SA as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMS SWISS LITHOCLAST LITHOTRIPTER?

The FDA product code for EMS SWISS LITHOCLAST LITHOTRIPTER is FFK.

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 Electro Medical Systems SA 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.

View all 9 devices →

Related Devices (Code: FFK)

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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