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FDA 510(k)

GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEED

K-Number: K914140 · 1992-03-31

ApplicantBissell Medical Products, Inc.
Decision Date1992-03-31
Product CodeFPP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEED is the device name listed in this FDA 510(k) record. The listed applicant is Bissell Medical Products, Inc.. It received FDA 510(k) clearance on 1992-03-31 under 510(k) number K914140. The device is classified under product code FPP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEED?

GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEED is a medical device that received FDA 510(k) clearance on 1992-03-31. The listed applicant is Bissell Medical Products, Inc.. The 510(k) number is K914140.

When did GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEED receive FDA 510(k) clearance?

GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEED received FDA 510(k) clearance on 1992-03-31, under 510(k) number K914140.

Who is the listed applicant for GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEED?

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

What is the FDA product code for GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEED?

The FDA product code for GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEED is FPP.

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 Bissell 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.

K932880GRASSI GASTROJEJUNOSTOMY TUBEK901683IMPROVED BAKER TWIN-CUFF SUMP TUBEK873441BAKER TWIN-CUFF INTESTINAL DECOMP/PLICATION TUBEK871691MODIFIED MULTI-LUMEN NASOGASTRIC TUBEK851672NYHUS/NELSON TUBE

Related Devices (Code: FPP)

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.

K030283BABY PODPrism Enterprises, Inc.K942356MED-EVAC-4 MEDICAL EVACUATION STRETCHERMontery Bay Corp.K940130STRYKER MODEL 6110 EMERGENCY/POLE STRETCHERStryker Corp.K940245EVACU-SLEDEvacu Technologies, Inc.K924275RESTRAINING STRETCHERDmsK922816U P CUSTOM DESIGN, INC. COT EQUIPMENT CARRIERUp Custom Design, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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