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)

REMOTE CONTROL SYSTEM FOR MICROSCOPE

K-Number: K760696 · 1976-12-16

Decision Date1976-12-16
Product CodeEPT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

REMOTE CONTROL SYSTEM FOR MICROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories. It received FDA 510(k) clearance on 1976-12-16 under 510(k) number K760696. The device is classified under product code EPT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REMOTE CONTROL SYSTEM FOR MICROSCOPE?

REMOTE CONTROL SYSTEM FOR MICROSCOPE is a medical device that received FDA 510(k) clearance on 1976-12-16. The listed applicant is Alcon Laboratories. The 510(k) number is K760696.

When did REMOTE CONTROL SYSTEM FOR MICROSCOPE receive FDA 510(k) clearance?

REMOTE CONTROL SYSTEM FOR MICROSCOPE received FDA 510(k) clearance on 1976-12-16, under 510(k) number K760696.

Who is the listed applicant for REMOTE CONTROL SYSTEM FOR MICROSCOPE?

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 REMOTE CONTROL SYSTEM FOR MICROSCOPE?

The FDA product code for REMOTE CONTROL SYSTEM FOR MICROSCOPE is EPT.

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: EPT)

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.

↑