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FDA 510(k)

2500 PRINTER

K-Number: K860164 · 1986-06-05

ApplicantDatascope Corp.
Decision Date1986-06-05
Product Code
DecisionSubstantially Equivalent

Device Summary

2500 PRINTER is the device name listed in this FDA 510(k) record. The listed applicant is Datascope Corp.. It received FDA 510(k) clearance on 1986-06-05 under 510(k) number K860164. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 2500 PRINTER?

2500 PRINTER is a medical device that received FDA 510(k) clearance on 1986-06-05. The listed applicant is Datascope Corp.. The 510(k) number is K860164.

When did 2500 PRINTER receive FDA 510(k) clearance?

2500 PRINTER received FDA 510(k) clearance on 1986-06-05, under 510(k) number K860164.

Who is the listed applicant for 2500 PRINTER?

The FDA 510(k) record lists Datascope Corp. 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.

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Other records listing Datascope Corp. 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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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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