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FDA 510(k)

DAS 211

K-Number: K862593 · 1986-09-08

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1986-09-08
Product Code
DecisionSubstantially Equivalent

Device Summary

DAS 211 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 1986-09-08 under 510(k) number K862593. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAS 211?

DAS 211 is a medical device that received FDA 510(k) clearance on 1986-09-08. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K862593.

When did DAS 211 receive FDA 510(k) clearance?

DAS 211 received FDA 510(k) clearance on 1986-09-08, under 510(k) number K862593.

Who is the listed applicant for DAS 211?

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

Other records listing Philips Medical Systems (Cleveland), 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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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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