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FDA 510(k)

VIDEO PRINTER, MODEL 3200

K-Number: K860904 · 1986-03-28

Decision Date1986-03-28
Product CodeKQM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VIDEO PRINTER, MODEL 3200 is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1986-03-28 under 510(k) number K860904. The device is classified under product code KQM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIDEO PRINTER, MODEL 3200?

VIDEO PRINTER, MODEL 3200 is a medical device that received FDA 510(k) clearance on 1986-03-28. The listed applicant is Medline Industries, Inc.. The 510(k) number is K860904.

When did VIDEO PRINTER, MODEL 3200 receive FDA 510(k) clearance?

VIDEO PRINTER, MODEL 3200 received FDA 510(k) clearance on 1986-03-28, under 510(k) number K860904.

Who is the listed applicant for VIDEO PRINTER, MODEL 3200?

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

What is the FDA product code for VIDEO PRINTER, MODEL 3200?

The FDA product code for VIDEO PRINTER, MODEL 3200 is KQM.

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 Medline Industries, 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.

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Related Devices (Code: KQM)

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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