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FDA 510(k)

MANAN D BAG

K-Number: K980005 · 1998-01-30

ApplicantMedical Device Technologies, Inc.
Decision Date1998-01-30
Product CodeEXF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MANAN D BAG is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Technologies, Inc.. It received FDA 510(k) clearance on 1998-01-30 under 510(k) number K980005. The device is classified under product code EXF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MANAN D BAG?

MANAN D BAG is a medical device that received FDA 510(k) clearance on 1998-01-30. The listed applicant is Medical Device Technologies, Inc.. The 510(k) number is K980005.

When did MANAN D BAG receive FDA 510(k) clearance?

MANAN D BAG received FDA 510(k) clearance on 1998-01-30, under 510(k) number K980005.

Who is the listed applicant for MANAN D BAG?

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

What is the FDA product code for MANAN D BAG?

The FDA product code for MANAN D BAG is EXF.

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Other records listing Medical Device 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.

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Related Devices (Code: EXF)

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.

K003078MERIT DRAINAGE DEPOTMerit Medical Systems, Inc.K990428DRAINAGE BAGRemington Medical, Inc.K961986MANAN D BAGManan Medical Products, Inc.K963849MANAN D BAGManan Medical Products, Inc.K943663NAVARRE 600 ML DRAINAGE BAGNavarre Biomedical , Ltd.K911129MMG BILE BAGMedical Technologies of Georgia

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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