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FDA 510(k)

BODYSCREEN II

K-Number: K843851 · 1985-02-14

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

Device Summary

BODYSCREEN II 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 K843851. 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 BODYSCREEN II?

BODYSCREEN II 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 K843851.

When did BODYSCREEN II receive FDA 510(k) clearance?

BODYSCREEN II received FDA 510(k) clearance on 1985-02-14, under 510(k) number K843851.

Who is the listed applicant for BODYSCREEN II?

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 BODYSCREEN II?

The FDA product code for BODYSCREEN II is CCM.

Related Clinical Trials

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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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