KSEA MODEL 203200 20 UNIMAT
K-Number: K953190 · 1995-10-05
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Device Summary
Frequently Asked Questions
What is the KSEA MODEL 203200 20 UNIMAT?
KSEA MODEL 203200 20 UNIMAT is a medical device that received FDA 510(k) clearance on 1995-10-05. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K953190.
When did KSEA MODEL 203200 20 UNIMAT receive FDA 510(k) clearance?
KSEA MODEL 203200 20 UNIMAT received FDA 510(k) clearance on 1995-10-05, under 510(k) number K953190.
Who is the listed applicant for KSEA MODEL 203200 20 UNIMAT?
The FDA 510(k) record lists KARL STORZ Endoscopy-America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KSEA MODEL 203200 20 UNIMAT?
The FDA product code for KSEA MODEL 203200 20 UNIMAT is HET.
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 KARL STORZ Endoscopy-America, 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.
Related Devices (Code: HET)
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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