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FDA 510(k)

UNIVERSAL-BODYTEST

K-Number: K843846 · 1985-02-14

ApplicantErich Jaeger, Inc.
Decision Date1985-02-14
Product CodeCCM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL-BODYTEST is the device name listed in this FDA 510(k) record. The listed applicant is Erich Jaeger, Inc.. It received FDA 510(k) clearance on 1985-02-14 under 510(k) number K843846. 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 UNIVERSAL-BODYTEST?

UNIVERSAL-BODYTEST is a medical device that received FDA 510(k) clearance on 1985-02-14. The listed applicant is Erich Jaeger, Inc.. The 510(k) number is K843846.

When did UNIVERSAL-BODYTEST receive FDA 510(k) clearance?

UNIVERSAL-BODYTEST received FDA 510(k) clearance on 1985-02-14, under 510(k) number K843846.

Who is the listed applicant for UNIVERSAL-BODYTEST?

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

What is the FDA product code for UNIVERSAL-BODYTEST?

The FDA product code for UNIVERSAL-BODYTEST is CCM.

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Other records listing Erich Jaeger, 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.

K000396APNOESCREEN PRO, ALPHA SCREEN PROK972419TOENNIES NEUROSCREEN SYSTEMK960078ASTHMA MONITORK932744FLOWSCREENK933839MASTER SCREEN PNUEMOK853443ALVEO-DIFFUSION TEST

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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.K852102COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEMWarren E. Collins, Inc.

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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