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FDA 510(k)

SWISS LITHOCLAST MULTIPURPOSE PROBE

K-Number: K992251 · 1999-07-27

Decision Date1999-07-27
Product CodeFFK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SWISS LITHOCLAST MULTIPURPOSE PROBE 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 1999-07-27 under 510(k) number K992251. 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 SWISS LITHOCLAST MULTIPURPOSE PROBE?

SWISS LITHOCLAST MULTIPURPOSE PROBE is a medical device that received FDA 510(k) clearance on 1999-07-27. The listed applicant is Electro Medical Systems SA. The 510(k) number is K992251.

When did SWISS LITHOCLAST MULTIPURPOSE PROBE receive FDA 510(k) clearance?

SWISS LITHOCLAST MULTIPURPOSE PROBE received FDA 510(k) clearance on 1999-07-27, under 510(k) number K992251.

Who is the listed applicant for SWISS LITHOCLAST MULTIPURPOSE PROBE?

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 SWISS LITHOCLAST MULTIPURPOSE PROBE?

The FDA product code for SWISS LITHOCLAST MULTIPURPOSE PROBE 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

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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