MARCO, MARCOTILT, ENCORE AND CUSTOM CHAIR
K-Number: K930449 · 1993-07-06
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Device Summary
Frequently Asked Questions
What is the MARCO, MARCOTILT, ENCORE AND CUSTOM CHAIR?
MARCO, MARCOTILT, ENCORE AND CUSTOM CHAIR is a medical device that received FDA 510(k) clearance on 1993-07-06. The listed applicant is Marco Ophthalmic, Inc.. The 510(k) number is K930449.
When did MARCO, MARCOTILT, ENCORE AND CUSTOM CHAIR receive FDA 510(k) clearance?
MARCO, MARCOTILT, ENCORE AND CUSTOM CHAIR received FDA 510(k) clearance on 1993-07-06, under 510(k) number K930449.
Who is the listed applicant for MARCO, MARCOTILT, ENCORE AND CUSTOM CHAIR?
The FDA 510(k) record lists Marco Ophthalmic, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MARCO, MARCOTILT, ENCORE AND CUSTOM CHAIR?
The FDA product code for MARCO, MARCOTILT, ENCORE AND CUSTOM CHAIR is HME.
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 Marco Ophthalmic, 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: HME)
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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