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FDA 510(k)

RS-RESIDUAL VOLUME SYSTEM

K-Number: K831778 · 1983-08-31

ApplicantWarren E. Collins, Inc.
Decision Date1983-08-31
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RS-RESIDUAL VOLUME SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Warren E. Collins, Inc.. It received FDA 510(k) clearance on 1983-08-31 under 510(k) number K831778. The device is classified under product code BZC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RS-RESIDUAL VOLUME SYSTEM?

RS-RESIDUAL VOLUME SYSTEM is a medical device that received FDA 510(k) clearance on 1983-08-31. The listed applicant is Warren E. Collins, Inc.. The 510(k) number is K831778.

When did RS-RESIDUAL VOLUME SYSTEM receive FDA 510(k) clearance?

RS-RESIDUAL VOLUME SYSTEM received FDA 510(k) clearance on 1983-08-31, under 510(k) number K831778.

Who is the listed applicant for RS-RESIDUAL VOLUME SYSTEM?

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

What is the FDA product code for RS-RESIDUAL VOLUME SYSTEM?

The FDA product code for RS-RESIDUAL VOLUME SYSTEM is BZC.

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Other records listing Warren E. Collins, 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.

K925459GS-MODULAR (GOLD STANDARD - MODULAR)K912946COLLINS DIGITAL PULMONARY MANOMETERK871151THE SPIRA ELEKTRO 2K861227COLLINS PNEUMOTACH PFT SYSTEMK852102COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEMK831780METABOLIC EXERCISE TESTING SYSTEM

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Related Devices (Code: BZC)

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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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