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FDA 510(k)

PMA ANGIOGRAPHY TRAY

K-Number: K841468 · 1984-06-05

Decision Date1984-06-05
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PMA ANGIOGRAPHY TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Professional Medical Services. It received FDA 510(k) clearance on 1984-06-05 under 510(k) number K841468. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PMA ANGIOGRAPHY TRAY?

PMA ANGIOGRAPHY TRAY is a medical device that received FDA 510(k) clearance on 1984-06-05. The listed applicant is Professional Medical Services. The 510(k) number is K841468.

When did PMA ANGIOGRAPHY TRAY receive FDA 510(k) clearance?

PMA ANGIOGRAPHY TRAY received FDA 510(k) clearance on 1984-06-05, under 510(k) number K841468.

Who is the listed applicant for PMA ANGIOGRAPHY TRAY?

The FDA 510(k) record lists Professional Medical Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PMA ANGIOGRAPHY TRAY?

The FDA product code for PMA ANGIOGRAPHY TRAY is DWS.

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 Professional Medical Services 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.

View all 19 devices →

Related Devices (Code: DWS)

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

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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