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)

TREADMILL MODEL 3060

K-Number: K792661 · 1980-02-19

Decision Date1980-02-19
Product CodeIOL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TREADMILL MODEL 3060 is the device name listed in this FDA 510(k) record. The listed applicant is Cambridge Instruments, Inc.. It received FDA 510(k) clearance on 1980-02-19 under 510(k) number K792661. The device is classified under product code IOL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TREADMILL MODEL 3060?

TREADMILL MODEL 3060 is a medical device that received FDA 510(k) clearance on 1980-02-19. The listed applicant is Cambridge Instruments, Inc.. The 510(k) number is K792661.

When did TREADMILL MODEL 3060 receive FDA 510(k) clearance?

TREADMILL MODEL 3060 received FDA 510(k) clearance on 1980-02-19, under 510(k) number K792661.

Who is the listed applicant for TREADMILL MODEL 3060?

The FDA 510(k) record lists Cambridge Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TREADMILL MODEL 3060?

The FDA product code for TREADMILL MODEL 3060 is IOL.

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 Cambridge Instruments, 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.

View all 13 devices →

Related Devices (Code: IOL)

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.

↑