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FDA 510(k)

MICROFIL CONTOURING INSTRUMENTS

K-Number: K830776 · 1983-04-28

Decision Date1983-04-28
Product CodeEIY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MICROFIL CONTOURING INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Almore Intl., Inc.. It received FDA 510(k) clearance on 1983-04-28 under 510(k) number K830776. The device is classified under product code EIY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROFIL CONTOURING INSTRUMENTS?

MICROFIL CONTOURING INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1983-04-28. The listed applicant is Almore Intl., Inc.. The 510(k) number is K830776.

When did MICROFIL CONTOURING INSTRUMENTS receive FDA 510(k) clearance?

MICROFIL CONTOURING INSTRUMENTS received FDA 510(k) clearance on 1983-04-28, under 510(k) number K830776.

Who is the listed applicant for MICROFIL CONTOURING INSTRUMENTS?

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

What is the FDA product code for MICROFIL CONTOURING INSTRUMENTS?

The FDA product code for MICROFIL CONTOURING INSTRUMENTS is EIY.

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 Almore Intl., 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 21 devices →

Related Devices (Code: EIY)

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.

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