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FDA 510(k)

PATIENT MONITOR RIGEL MODEL MULTICARE 429

K-Number: K884645 · 1989-02-02

ApplicantRigel Medical Electronics, Inc.
Decision Date1989-02-02
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PATIENT MONITOR RIGEL MODEL MULTICARE 429 is the device name listed in this FDA 510(k) record. The listed applicant is Rigel Medical Electronics, Inc.. It received FDA 510(k) clearance on 1989-02-02 under 510(k) number K884645. 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 PATIENT MONITOR RIGEL MODEL MULTICARE 429?

PATIENT MONITOR RIGEL MODEL MULTICARE 429 is a medical device that received FDA 510(k) clearance on 1989-02-02. The listed applicant is Rigel Medical Electronics, Inc.. The 510(k) number is K884645.

When did PATIENT MONITOR RIGEL MODEL MULTICARE 429 receive FDA 510(k) clearance?

PATIENT MONITOR RIGEL MODEL MULTICARE 429 received FDA 510(k) clearance on 1989-02-02, under 510(k) number K884645.

Who is the listed applicant for PATIENT MONITOR RIGEL MODEL MULTICARE 429?

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

What is the FDA product code for PATIENT MONITOR RIGEL MODEL MULTICARE 429?

The FDA product code for PATIENT MONITOR RIGEL MODEL MULTICARE 429 is DRT.

Related Clinical Trials

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Other records listing Rigel Medical Electronics, 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.

K875160RIGEL MODEL MULTICARE 409K850407NEONATAL MONITOR 309K850156ECG PATIENT MONITOR 301K850155ECG PATIENT MONITOR 302K843376ECG PATIENT MONITOR

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

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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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