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FDA 510(k)

EXCALIBUR ELECTROSURGICAL UNIT 60-5200-001

K-Number: K873809 · 1987-11-20

Decision Date1987-11-20
Product CodeBWA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EXCALIBUR ELECTROSURGICAL UNIT 60-5200-001 is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer Aspen Labs. It received FDA 510(k) clearance on 1987-11-20 under 510(k) number K873809. The device is classified under product code BWA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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