Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SORING GMBH SONOCA 180/190

K-Number: K012753 · 2001-11-13

Decision Date2001-11-13
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

SORING GMBH SONOCA 180/190 is the device name listed in this FDA 510(k) record. The listed applicant is Soring GmbH Medizintechnik. It received FDA 510(k) clearance on 2001-11-13 under 510(k) number K012753. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SORING GMBH SONOCA 180/190?

SORING GMBH SONOCA 180/190 is a medical device that received FDA 510(k) clearance on 2001-11-13. The listed applicant is Soring GmbH Medizintechnik. The 510(k) number is K012753.

When did SORING GMBH SONOCA 180/190 receive FDA 510(k) clearance?

SORING GMBH SONOCA 180/190 received FDA 510(k) clearance on 2001-11-13, under 510(k) number K012753.

Who is the listed applicant for SORING GMBH SONOCA 180/190?

The FDA 510(k) record lists Soring GmbH Medizintechnik as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SORING GMBH SONOCA 180/190?

The FDA product code for SORING GMBH SONOCA 180/190 is LFL.

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 Soring GmbH Medizintechnik 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 7 devices →

Related Devices (Code: LFL)

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.

↑