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FDA 510(k)

MANAN D BAG

K-Number: K963849 · 1996-12-13

ApplicantManan Medical Products, Inc.
Decision Date1996-12-13
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 Manan Medical Products, Inc.. It received FDA 510(k) clearance on 1996-12-13 under 510(k) number K963849. 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 1996-12-13. The listed applicant is Manan Medical Products, Inc.. The 510(k) number is K963849.

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

MANAN D BAG received FDA 510(k) clearance on 1996-12-13, under 510(k) number K963849.

Who is the listed applicant for MANAN D BAG?

The FDA 510(k) record lists Manan Medical Products, 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.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Manan Medical Products, 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.

K052802MANAN BIO-CUT SOFT TISSUE BIOPSY NEEDLEK011209MANAN SPRITACRE SPINAL NEEDLESK983620MANAN SPINAL NEEDLESK980536EPIDURAL NEEDLEK981386MANAN BLUNT NEEDLEK980211MRI CHIBA,SPINAL,BREAST LOCALIZATION,AUTOMATIC CUTTING NEEDLES

View all 39 devices →

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.K980005MANAN D BAGMedical Device Technologies, Inc.K961986MANAN 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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