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FDA 510(k)

MAGNUM 800(TM) MANAGEMENT SYSTEM

K-Number: K881844 · 1988-07-14

ApplicantThe Medical Group, Inc.
Decision Date1988-07-14
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MAGNUM 800(TM) MANAGEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is The Medical Group, Inc.. It received FDA 510(k) clearance on 1988-07-14 under 510(k) number K881844. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGNUM 800(TM) MANAGEMENT SYSTEM?

MAGNUM 800(TM) MANAGEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1988-07-14. The listed applicant is The Medical Group, Inc.. The 510(k) number is K881844.

When did MAGNUM 800(TM) MANAGEMENT SYSTEM receive FDA 510(k) clearance?

MAGNUM 800(TM) MANAGEMENT SYSTEM received FDA 510(k) clearance on 1988-07-14, under 510(k) number K881844.

Who is the listed applicant for MAGNUM 800(TM) MANAGEMENT SYSTEM?

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

What is the FDA product code for MAGNUM 800(TM) MANAGEMENT SYSTEM?

The FDA product code for MAGNUM 800(TM) MANAGEMENT SYSTEM is FNL.

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Other records listing The Medical Group, 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.

K911246THE MEDISCUS PEDCARE MANAGEMENT SYSTEM-MODEL 2K901295PULMONAIR 40 PATIENT MANAGEMENT SYSTEMK881843PEDIATRIC HOSPITAL BEDK870284TRIANGULAR BANDAGEK8702824 X 4 SPONGES, NON-STERILEK8702833 X 3 SPONGES, NON-STERILE

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Related Devices (Code: FNL)

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.

K202964iBed Wireless with iBed MobileStryker CorporationK103536IBED WIRELESS WITH IBED AWARENESSStryker CorporationK982783VAIL 1000 ENCLOSED BEDVail Products, Inc.K974296MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BEDInvacare Corp.K974254BENEFIT B3--- SERIESM.C. Healthcare Products, Inc.K972115VOLKER HOSPITAL BED, MODEL K960Volker Healthcare, Inc.

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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