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FDA 510(k)

MODULAP

K-Number: K983623 · 1998-12-18

Decision Date1998-12-18
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODULAP is the device name listed in this FDA 510(k) record. The listed applicant is Atc Technologies, Inc.. It received FDA 510(k) clearance on 1998-12-18 under 510(k) number K983623. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

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

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