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FDA 510(k)

TRENDO-SCOPE

K-Number: K831995 · 1983-08-08

ApplicantGabriel Ent.
Decision Date1983-08-08
Product CodeHCS
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TRENDO-SCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Gabriel Ent.. It received FDA 510(k) clearance on 1983-08-08 under 510(k) number K831995. The device is classified under product code HCS. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRENDO-SCOPE?

TRENDO-SCOPE is a medical device that received FDA 510(k) clearance on 1983-08-08. The listed applicant is Gabriel Ent.. The 510(k) number is K831995.

When did TRENDO-SCOPE receive FDA 510(k) clearance?

TRENDO-SCOPE received FDA 510(k) clearance on 1983-08-08, under 510(k) number K831995.

Who is the listed applicant for TRENDO-SCOPE?

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

What is the FDA product code for TRENDO-SCOPE?

The FDA product code for TRENDO-SCOPE is HCS.

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 Gabriel Ent. 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: HCS)

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

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