KSEA DE LA PLAZA BLEPHAROPLASTY SET
K-Number: K991592 · 1999-11-02
Advertisement
Device Summary
Frequently Asked Questions
What is the KSEA DE LA PLAZA BLEPHAROPLASTY SET?
KSEA DE LA PLAZA BLEPHAROPLASTY SET is a medical device that received FDA 510(k) clearance on 1999-11-02. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K991592.
When did KSEA DE LA PLAZA BLEPHAROPLASTY SET receive FDA 510(k) clearance?
KSEA DE LA PLAZA BLEPHAROPLASTY SET received FDA 510(k) clearance on 1999-11-02, under 510(k) number K991592.
Who is the listed applicant for KSEA DE LA PLAZA BLEPHAROPLASTY SET?
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 DE LA PLAZA BLEPHAROPLASTY SET?
The FDA product code for KSEA DE LA PLAZA BLEPHAROPLASTY SET is HNI.
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: HNI)
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.
Advertisement