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)

TED MODEL 760

K-Number: K871828 · 1988-02-04

Decision Date1988-02-04
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TED MODEL 760 is the device name listed in this FDA 510(k) record. The listed applicant is Teledyne, Inc.. It received FDA 510(k) clearance on 1988-02-04 under 510(k) number K871828. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TED MODEL 760?

TED MODEL 760 is a medical device that received FDA 510(k) clearance on 1988-02-04. The listed applicant is Teledyne, Inc.. The 510(k) number is K871828.

When did TED MODEL 760 receive FDA 510(k) clearance?

TED MODEL 760 received FDA 510(k) clearance on 1988-02-04, under 510(k) number K871828.

Who is the listed applicant for TED MODEL 760?

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

What is the FDA product code for TED MODEL 760?

The FDA product code for TED MODEL 760 is CCK.

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 Teledyne, 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 10 devices →

Related Devices (Code: CCK)

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.

↑