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FDA 510(k)

MS PAED-BABY BODY

K-Number: K023796 · 2003-03-03

ApplicantErich Jaeger GmbH
Decision Date2003-03-03
Product CodeCCM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MS PAED-BABY BODY is the device name listed in this FDA 510(k) record. The listed applicant is Erich Jaeger GmbH. It received FDA 510(k) clearance on 2003-03-03 under 510(k) number K023796. 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 MS PAED-BABY BODY?

MS PAED-BABY BODY is a medical device that received FDA 510(k) clearance on 2003-03-03. The listed applicant is Erich Jaeger GmbH. The 510(k) number is K023796.

When did MS PAED-BABY BODY receive FDA 510(k) clearance?

MS PAED-BABY BODY received FDA 510(k) clearance on 2003-03-03, under 510(k) number K023796.

Who is the listed applicant for MS PAED-BABY BODY?

The FDA 510(k) record lists Erich Jaeger GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MS PAED-BABY BODY?

The FDA product code for MS PAED-BABY BODY is CCM.

Other records listing Erich Jaeger GmbH 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.

K023120OXYCON MOBILEK021138SLEEPSCREEN/APNOESCREEN CARDIOK001502AEROSOL PROVOCATION SYSTEM APS PRO, MODEL APS PROK000648SPIRO PRO

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 GmbHK9432591085 ULTIMATE E PLETHYSMOGRAPHMedical Graphics Corp.K893420MASTERLAB PFT AND MASTERLAB BODY BOXQuinton, Inc.K853390INFANT BODY TESTErich Jaeger, Inc.K852102COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEMWarren E. Collins, 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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