SWISS LITHOCLAST LITHOTRIPTER
K-Number: K951531 · 1995-08-24
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Device Summary
Frequently Asked Questions
What is the SWISS LITHOCLAST LITHOTRIPTER?
SWISS LITHOCLAST LITHOTRIPTER is a medical device that received FDA 510(k) clearance on 1995-08-24. The listed applicant is Electro Medical Systems SA. The 510(k) number is K951531.
When did SWISS LITHOCLAST LITHOTRIPTER receive FDA 510(k) clearance?
SWISS LITHOCLAST LITHOTRIPTER received FDA 510(k) clearance on 1995-08-24, under 510(k) number K951531.
Who is the listed applicant for 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 SWISS LITHOCLAST LITHOTRIPTER?
The FDA product code for 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.
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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