MODULAP
K-Number: K983623 · 1998-12-18
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Device Summary
Frequently Asked Questions
What is the MODULAP?
MODULAP is a medical device that received FDA 510(k) clearance on 1998-12-18. The listed applicant is Atc Technologies, Inc.. The 510(k) number is K983623.
When did MODULAP receive FDA 510(k) clearance?
MODULAP received FDA 510(k) clearance on 1998-12-18, under 510(k) number K983623.
Who is the listed applicant for MODULAP?
The FDA 510(k) record lists Atc Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODULAP?
The FDA product code for MODULAP is GCJ.
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 Atc Technologies, 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: GCJ)
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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