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FDA 510(k)

MEDI-TRACE PHYSIOLOGICAL PRESSURE TRANS

K-Number: K820457 · 1982-03-12

Decision Date1982-03-12
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDI-TRACE PHYSIOLOGICAL PRESSURE TRANS is the device name listed in this FDA 510(k) record. The listed applicant is Graphic Controls Corp.. It received FDA 510(k) clearance on 1982-03-12 under 510(k) number K820457. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI-TRACE PHYSIOLOGICAL PRESSURE TRANS?

MEDI-TRACE PHYSIOLOGICAL PRESSURE TRANS is a medical device that received FDA 510(k) clearance on 1982-03-12. The listed applicant is Graphic Controls Corp.. The 510(k) number is K820457.

When did MEDI-TRACE PHYSIOLOGICAL PRESSURE TRANS receive FDA 510(k) clearance?

MEDI-TRACE PHYSIOLOGICAL PRESSURE TRANS received FDA 510(k) clearance on 1982-03-12, under 510(k) number K820457.

Who is the listed applicant for MEDI-TRACE PHYSIOLOGICAL PRESSURE TRANS?

The FDA 510(k) record lists Graphic Controls Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDI-TRACE PHYSIOLOGICAL PRESSURE TRANS?

The FDA product code for MEDI-TRACE PHYSIOLOGICAL PRESSURE TRANS is DRS.

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 Graphic Controls 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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Related Devices (Code: DRS)

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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