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FDA 510(k)

MODEL ICPM & ACCESSORIES

K-Number: K823681 · 1983-02-23

Decision Date1983-02-23
Product CodeJFC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL ICPM & ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Electromedics, Inc.. It received FDA 510(k) clearance on 1983-02-23 under 510(k) number K823681. The device is classified under product code JFC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL ICPM & ACCESSORIES?

MODEL ICPM & ACCESSORIES is a medical device that received FDA 510(k) clearance on 1983-02-23. The listed applicant is Electromedics, Inc.. The 510(k) number is K823681.

When did MODEL ICPM & ACCESSORIES receive FDA 510(k) clearance?

MODEL ICPM & ACCESSORIES received FDA 510(k) clearance on 1983-02-23, under 510(k) number K823681.

Who is the listed applicant for MODEL ICPM & ACCESSORIES?

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

What is the FDA product code for MODEL ICPM & ACCESSORIES?

The FDA product code for MODEL ICPM & ACCESSORIES is JFC.

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 Electromedics, 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 41 devices →

Related Devices (Code: JFC)

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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