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FDA 510(k)

COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEM

K-Number: K852102 · 1985-07-31

ApplicantWarren E. Collins, Inc.
Decision Date1985-07-31
Product CodeCCM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

COLLIN BODY PLETHYSMOGRAPH PLUS 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 1985-07-31 under 510(k) number K852102. The device is classified under product code CCM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEM?

COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEM is a medical device that received FDA 510(k) clearance on 1985-07-31. The listed applicant is Warren E. Collins, Inc.. The 510(k) number is K852102.

When did COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEM receive FDA 510(k) clearance?

COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEM received FDA 510(k) clearance on 1985-07-31, under 510(k) number K852102.

Who is the listed applicant for COLLIN BODY PLETHYSMOGRAPH PLUS 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 COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEM?

The FDA product code for COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEM is CCM.

Related Clinical Trials

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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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 SYSTEMK831780METABOLIC EXERCISE TESTING SYSTEMK831778RS-RESIDUAL VOLUME SYSTEM

View all 14 devices →

Related Devices (Code: CCM)

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.

K081823MASTERSCREEN PAED - BABY BODYViasys Healthcare GmbHK023796MS PAED-BABY BODYErich Jaeger GmbHK9432591085 ULTIMATE E PLETHYSMOGRAPHMedical Graphics Corp.K893420MASTERLAB PFT AND MASTERLAB BODY BOXQuinton, Inc.K853390INFANT BODY TESTErich Jaeger, Inc.K852088SYSTEM 1085 BODY PLETHYSMOGRAPHMedical Graphics Corp.

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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