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FDA 510(k)

DISPOSABLE DOME STOCK #D-300

K-Number: K884919 · 1989-01-05

ApplicantAdvanced Medical, Inc.
Decision Date1989-01-05
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE DOME STOCK #D-300 is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Medical, Inc.. It received FDA 510(k) clearance on 1989-01-05 under 510(k) number K884919. 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 DISPOSABLE DOME STOCK #D-300?

DISPOSABLE DOME STOCK #D-300 is a medical device that received FDA 510(k) clearance on 1989-01-05. The listed applicant is Advanced Medical, Inc.. The 510(k) number is K884919.

When did DISPOSABLE DOME STOCK #D-300 receive FDA 510(k) clearance?

DISPOSABLE DOME STOCK #D-300 received FDA 510(k) clearance on 1989-01-05, under 510(k) number K884919.

Who is the listed applicant for DISPOSABLE DOME STOCK #D-300?

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

What is the FDA product code for DISPOSABLE DOME STOCK #D-300?

The FDA product code for DISPOSABLE DOME STOCK #D-300 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.

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Other records listing Advanced Medical, 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.

K871493DENTI-TRAY(TM)K760368MONITORING & STRESS TESTING EQUIPMENT

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.

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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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