POSTURE MIRROR
K-Number: K812479 · 1981-12-09
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Device Summary
Frequently Asked Questions
What is the POSTURE MIRROR?
POSTURE MIRROR is a medical device that received FDA 510(k) clearance on 1981-12-09. The listed applicant is Maddak, Inc.. The 510(k) number is K812479.
When did POSTURE MIRROR receive FDA 510(k) clearance?
POSTURE MIRROR received FDA 510(k) clearance on 1981-12-09, under 510(k) number K812479.
Who is the listed applicant for POSTURE MIRROR?
The FDA 510(k) record lists Maddak, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POSTURE MIRROR?
The FDA product code for POSTURE MIRROR is LDQ.
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 Maddak, 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: LDQ)
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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