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FDA 510(k)

RM-301 PATIENT MONITOR

K-Number: K880498 · 1988-05-13

ApplicantPpg Industries, Inc.
Decision Date1988-05-13
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RM-301 PATIENT MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Ppg Industries, Inc.. It received FDA 510(k) clearance on 1988-05-13 under 510(k) number K880498. 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 RM-301 PATIENT MONITOR?

RM-301 PATIENT MONITOR is a medical device that received FDA 510(k) clearance on 1988-05-13. The listed applicant is Ppg Industries, Inc.. The 510(k) number is K880498.

When did RM-301 PATIENT MONITOR receive FDA 510(k) clearance?

RM-301 PATIENT MONITOR received FDA 510(k) clearance on 1988-05-13, under 510(k) number K880498.

Who is the listed applicant for RM-301 PATIENT MONITOR?

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

What is the FDA product code for RM-301 PATIENT MONITOR?

The FDA product code for RM-301 PATIENT MONITOR is DRT.

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Other records listing Ppg Industries, Inc. as applicant

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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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