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FDA 510(k)

NUMOBAG

K-Number: K981949 · 1999-02-03

ApplicantNumotech, Inc.
Decision Date1999-02-03
Product CodeKPJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NUMOBAG is the device name listed in this FDA 510(k) record. The listed applicant is Numotech, Inc.. It received FDA 510(k) clearance on 1999-02-03 under 510(k) number K981949. The device is classified under product code KPJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUMOBAG?

NUMOBAG is a medical device that received FDA 510(k) clearance on 1999-02-03. The listed applicant is Numotech, Inc.. The 510(k) number is K981949.

When did NUMOBAG receive FDA 510(k) clearance?

NUMOBAG received FDA 510(k) clearance on 1999-02-03, under 510(k) number K981949.

Who is the listed applicant for NUMOBAG?

The FDA 510(k) record lists Numotech, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NUMOBAG?

The FDA product code for NUMOBAG is KPJ.

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.

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Other records listing Numotech, 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.

K943433TOTAL CONTACT SEAT RIPPLE SYSTEM

Related Devices (Code: KPJ)

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.

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Official Source

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