EXCALIBUR ELECTROSURGICAL UNIT 60-5200-001
K-Number: K873809 · 1987-11-20
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Device Summary
Frequently Asked Questions
What is the EXCALIBUR ELECTROSURGICAL UNIT 60-5200-001?
EXCALIBUR ELECTROSURGICAL UNIT 60-5200-001 is a medical device that received FDA 510(k) clearance on 1987-11-20. The listed applicant is Zimmer Aspen Labs. The 510(k) number is K873809.
When did EXCALIBUR ELECTROSURGICAL UNIT 60-5200-001 receive FDA 510(k) clearance?
EXCALIBUR ELECTROSURGICAL UNIT 60-5200-001 received FDA 510(k) clearance on 1987-11-20, under 510(k) number K873809.
Who is the listed applicant for EXCALIBUR ELECTROSURGICAL UNIT 60-5200-001?
The FDA 510(k) record lists Zimmer Aspen Labs as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EXCALIBUR ELECTROSURGICAL UNIT 60-5200-001?
The FDA product code for EXCALIBUR ELECTROSURGICAL UNIT 60-5200-001 is BWA.
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.
Related Devices (Code: BWA)
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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