ATD AUTOMATIC BRIDGE REMOVER
K-Number: K992649 · 1999-10-29
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Device Summary
Frequently Asked Questions
What is the ATD AUTOMATIC BRIDGE REMOVER?
ATD AUTOMATIC BRIDGE REMOVER is a medical device that received FDA 510(k) clearance on 1999-10-29. The listed applicant is J. Morita USA, Inc.. The 510(k) number is K992649.
When did ATD AUTOMATIC BRIDGE REMOVER receive FDA 510(k) clearance?
ATD AUTOMATIC BRIDGE REMOVER received FDA 510(k) clearance on 1999-10-29, under 510(k) number K992649.
Who is the listed applicant for ATD AUTOMATIC BRIDGE REMOVER?
The FDA 510(k) record lists J. Morita USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ATD AUTOMATIC BRIDGE REMOVER?
The FDA product code for ATD AUTOMATIC BRIDGE REMOVER is EIS.
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 J. Morita USA, 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: EIS)
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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