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FDA 510(k)

PATIENT MONITOR PB240

K-Number: K853318 · 1986-03-11

ApplicantPuritan Bennett Corp.
Decision Date1986-03-11
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PATIENT MONITOR PB240 is the device name listed in this FDA 510(k) record. The listed applicant is Puritan Bennett Corp.. It received FDA 510(k) clearance on 1986-03-11 under 510(k) number K853318. 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 PB240?

PATIENT MONITOR PB240 is a medical device that received FDA 510(k) clearance on 1986-03-11. The listed applicant is Puritan Bennett Corp.. The 510(k) number is K853318.

When did PATIENT MONITOR PB240 receive FDA 510(k) clearance?

PATIENT MONITOR PB240 received FDA 510(k) clearance on 1986-03-11, under 510(k) number K853318.

Who is the listed applicant for PATIENT MONITOR PB240?

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

What is the FDA product code for PATIENT MONITOR PB240?

The FDA product code for PATIENT MONITOR PB240 is DRT.

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Other records listing Puritan Bennett 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.

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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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