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FDA 510(k)

SAC-RO-FORM INSERT & BINDER

K-Number: K830349 · 1983-03-09

Decision Date1983-03-09
Product Code
DecisionSubstantially Equivalent

Device Summary

SAC-RO-FORM INSERT & BINDER is the device name listed in this FDA 510(k) record. The listed applicant is Deip Enterprises, Inc.. It received FDA 510(k) clearance on 1983-03-09 under 510(k) number K830349. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAC-RO-FORM INSERT & BINDER?

SAC-RO-FORM INSERT & BINDER is a medical device that received FDA 510(k) clearance on 1983-03-09. The listed applicant is Deip Enterprises, Inc.. The 510(k) number is K830349.

When did SAC-RO-FORM INSERT & BINDER receive FDA 510(k) clearance?

SAC-RO-FORM INSERT & BINDER received FDA 510(k) clearance on 1983-03-09, under 510(k) number K830349.

Who is the listed applicant for SAC-RO-FORM INSERT & BINDER?

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

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 Deip Enterprises, 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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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