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)

KARL STORZ BOUGIES AND DILATORS

K-Number: K950125 · 1995-02-07

Decision Date1995-02-07
Product CodeFAX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KARL STORZ BOUGIES AND DILATORS is the device name listed in this FDA 510(k) record. The listed applicant is KARL STORZ Endoscopy-America, Inc.. It received FDA 510(k) clearance on 1995-02-07 under 510(k) number K950125. The device is classified under product code FAX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ BOUGIES AND DILATORS?

KARL STORZ BOUGIES AND DILATORS is a medical device that received FDA 510(k) clearance on 1995-02-07. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K950125.

When did KARL STORZ BOUGIES AND DILATORS receive FDA 510(k) clearance?

KARL STORZ BOUGIES AND DILATORS received FDA 510(k) clearance on 1995-02-07, under 510(k) number K950125.

Who is the listed applicant for KARL STORZ BOUGIES AND DILATORS?

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 KARL STORZ BOUGIES AND DILATORS?

The FDA product code for KARL STORZ BOUGIES AND DILATORS is FAX.

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.

View all 355 devices →

Related Devices (Code: FAX)

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.

↑