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FDA 510(k)

CABINET FOR MULTIPLE FUNCTION BLOCKS

K-Number: K830795 · 1983-05-18

ApplicantElectronics For Medicine, Inc.
Decision Date1983-05-18
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CABINET FOR MULTIPLE FUNCTION BLOCKS is the device name listed in this FDA 510(k) record. The listed applicant is Electronics For Medicine, Inc.. It received FDA 510(k) clearance on 1983-05-18 under 510(k) number K830795. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CABINET FOR MULTIPLE FUNCTION BLOCKS?

CABINET FOR MULTIPLE FUNCTION BLOCKS is a medical device that received FDA 510(k) clearance on 1983-05-18. The listed applicant is Electronics For Medicine, Inc.. The 510(k) number is K830795.

When did CABINET FOR MULTIPLE FUNCTION BLOCKS receive FDA 510(k) clearance?

CABINET FOR MULTIPLE FUNCTION BLOCKS received FDA 510(k) clearance on 1983-05-18, under 510(k) number K830795.

Who is the listed applicant for CABINET FOR MULTIPLE FUNCTION BLOCKS?

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

What is the FDA product code for CABINET FOR MULTIPLE FUNCTION BLOCKS?

The FDA product code for CABINET FOR MULTIPLE FUNCTION BLOCKS is DRT.

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Other records listing Electronics For Medicine, 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.

K830791UNIVERSAL MEDDARS SYSTEMK792528RESPIRATION/APNEA AMPLIFIER MODEL 3105K791006SMART BILECTRODESK790198MONITOR PLUG-IN MODEL M1106 ECGK790203INTERVAL TIMER MODEL V4295K790185MODEL V 4207 INTEGRATING PLUG-IN

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Related Devices (Code: DRT)

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.

K254058DistaSense(TM) (v1)Life Detection TechnologiesK261286The Circadia C300 System (C300)Circadia Health, Inc.K252676The Circadia C300 System (C300)Circadia Health, Inc.K253388Sleepiz One+ (Model 2.5)Sleepiz AGK251364Sleepiz One+ (2.5)Sleepiz AGK234003The Circadia C200 SystemCircadia Technologies, Ltd.

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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