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FDA 510(k)

ANDRIES PHYSICAL ASSESSMENT COMPUTER

K-Number: K870545 · 1987-08-14

Decision Date1987-08-14
Product CodeDQC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANDRIES PHYSICAL ASSESSMENT COMPUTER is the device name listed in this FDA 510(k) record. The listed applicant is Andries Tek, Inc.. It received FDA 510(k) clearance on 1987-08-14 under 510(k) number K870545. The device is classified under product code DQC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANDRIES PHYSICAL ASSESSMENT COMPUTER?

ANDRIES PHYSICAL ASSESSMENT COMPUTER is a medical device that received FDA 510(k) clearance on 1987-08-14. The listed applicant is Andries Tek, Inc.. The 510(k) number is K870545.

When did ANDRIES PHYSICAL ASSESSMENT COMPUTER receive FDA 510(k) clearance?

ANDRIES PHYSICAL ASSESSMENT COMPUTER received FDA 510(k) clearance on 1987-08-14, under 510(k) number K870545.

Who is the listed applicant for ANDRIES PHYSICAL ASSESSMENT COMPUTER?

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

What is the FDA product code for ANDRIES PHYSICAL ASSESSMENT COMPUTER?

The FDA product code for ANDRIES PHYSICAL ASSESSMENT COMPUTER is DQC.

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.

Related Devices (Code: DQC)

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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