ADAM (ACOUSTICAL DEVICE FOR ANATOMICAL MONITORING)
K-Number: K893557 · 1990-03-19
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Device Summary
Frequently Asked Questions
What is the ADAM (ACOUSTICAL DEVICE FOR ANATOMICAL MONITORING)?
ADAM (ACOUSTICAL DEVICE FOR ANATOMICAL MONITORING) is a medical device that received FDA 510(k) clearance on 1990-03-19. The listed applicant is Medical Monitors, Inc.. The 510(k) number is K893557.
When did ADAM (ACOUSTICAL DEVICE FOR ANATOMICAL MONITORING) receive FDA 510(k) clearance?
ADAM (ACOUSTICAL DEVICE FOR ANATOMICAL MONITORING) received FDA 510(k) clearance on 1990-03-19, under 510(k) number K893557.
Who is the listed applicant for ADAM (ACOUSTICAL DEVICE FOR ANATOMICAL MONITORING)?
The FDA 510(k) record lists Medical Monitors, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ADAM (ACOUSTICAL DEVICE FOR ANATOMICAL MONITORING)?
The FDA product code for ADAM (ACOUSTICAL DEVICE FOR ANATOMICAL MONITORING) is DQD.
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 Medical Monitors, 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.
Related Devices (Code: DQD)
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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