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FDA 510(k)

ALCON OPERATING MICROSCOPES

K-Number: K920641 · 1992-10-09

Decision Date1992-10-09
Product CodeHRM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ALCON OPERATING MICROSCOPES is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories. It received FDA 510(k) clearance on 1992-10-09 under 510(k) number K920641. The device is classified under product code HRM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALCON OPERATING MICROSCOPES?

ALCON OPERATING MICROSCOPES is a medical device that received FDA 510(k) clearance on 1992-10-09. The listed applicant is Alcon Laboratories. The 510(k) number is K920641.

When did ALCON OPERATING MICROSCOPES receive FDA 510(k) clearance?

ALCON OPERATING MICROSCOPES received FDA 510(k) clearance on 1992-10-09, under 510(k) number K920641.

Who is the listed applicant for ALCON OPERATING MICROSCOPES?

The FDA 510(k) record lists Alcon Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALCON OPERATING MICROSCOPES?

The FDA product code for ALCON OPERATING MICROSCOPES is HRM.

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 Alcon Laboratories 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 47 devices →

Related Devices (Code: HRM)

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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