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FDA 510(k)

AP900/PRP MODULE AND ACCESSORIES, MODIFICATION

K-Number: K893218 · 1990-06-12

ApplicantElectromedics, Inc.
Decision Date1990-06-12
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AP900/PRP MODULE AND ACCESSORIES, MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Electromedics, Inc.. It received FDA 510(k) clearance on 1990-06-12 under 510(k) number K893218. The device is classified under product code CAC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AP900/PRP MODULE AND ACCESSORIES, MODIFICATION?

AP900/PRP MODULE AND ACCESSORIES, MODIFICATION is a medical device that received FDA 510(k) clearance on 1990-06-12. The listed applicant is Electromedics, Inc.. The 510(k) number is K893218.

When did AP900/PRP MODULE AND ACCESSORIES, MODIFICATION receive FDA 510(k) clearance?

AP900/PRP MODULE AND ACCESSORIES, MODIFICATION received FDA 510(k) clearance on 1990-06-12, under 510(k) number K893218.

Who is the listed applicant for AP900/PRP MODULE AND ACCESSORIES, MODIFICATION?

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 AP900/PRP MODULE AND ACCESSORIES, MODIFICATION?

The FDA product code for AP900/PRP MODULE AND ACCESSORIES, MODIFICATION is CAC.

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Other records listing Electromedics, Inc. as applicant

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Related Devices (Code: CAC)

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.

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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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