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)

EXTENDED STRAIGHT ATTACHMENT

K-Number: K994024 · 2000-02-03

Decision Date2000-02-03
Product CodeEGS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EXTENDED STRAIGHT ATTACHMENT is the device name listed in this FDA 510(k) record. The listed applicant is Team Technologies, Inc.. It received FDA 510(k) clearance on 2000-02-03 under 510(k) number K994024. The device is classified under product code EGS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXTENDED STRAIGHT ATTACHMENT?

EXTENDED STRAIGHT ATTACHMENT is a medical device that received FDA 510(k) clearance on 2000-02-03. The listed applicant is Team Technologies, Inc.. The 510(k) number is K994024.

When did EXTENDED STRAIGHT ATTACHMENT receive FDA 510(k) clearance?

EXTENDED STRAIGHT ATTACHMENT received FDA 510(k) clearance on 2000-02-03, under 510(k) number K994024.

Who is the listed applicant for EXTENDED STRAIGHT ATTACHMENT?

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

What is the FDA product code for EXTENDED STRAIGHT ATTACHMENT?

The FDA product code for EXTENDED STRAIGHT ATTACHMENT is EGS.

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 Team Technologies, 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.

Related Devices (Code: EGS)

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.

↑