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FDA 510(k)

MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BED

K-Number: K974296 · 1998-01-06

ApplicantInvacare Corp.
Decision Date1998-01-06
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BED is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 1998-01-06 under 510(k) number K974296. 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 MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BED?

MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BED is a medical device that received FDA 510(k) clearance on 1998-01-06. The listed applicant is Invacare Corp.. The 510(k) number is K974296.

When did MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BED receive FDA 510(k) clearance?

MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BED received FDA 510(k) clearance on 1998-01-06, under 510(k) number K974296.

Who is the listed applicant for MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BED?

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

What is the FDA product code for MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BED?

The FDA product code for MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BED is FNL.

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Other records listing Invacare Corp. 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.

K071928THE INVACARE FLYER, MODEL IPC 100K070321TWILIGHT FULL FACE MASKK062402EASYSTAND EVOLVK061874INVACARE'S TWILIGHT II NASAL MASKSK033819INVACARE 3G TARSYSK031176INVACARE POLARIS EX HEATED HUMIDIFIER, MODEL ISP4000

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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.K974254BENEFIT B3--- SERIESM.C. Healthcare Products, Inc.K972115VOLKER HOSPITAL BED, MODEL K960Volker Healthcare, Inc.K971546SOMA 900 TRANSPORT BEDNova Technologies, 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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