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FDA 510(k)

BODYLOG ENHANCED STRESS REDUCTION PACKAGE

K-Number: K902450 · 1991-01-25

ApplicantBodylog, Inc.
Decision Date1991-01-25
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

BODYLOG ENHANCED STRESS REDUCTION PACKAGE is the device name listed in this FDA 510(k) record. The listed applicant is Bodylog, Inc.. It received FDA 510(k) clearance on 1991-01-25 under 510(k) number K902450. The device is classified under product code HCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BODYLOG ENHANCED STRESS REDUCTION PACKAGE?

BODYLOG ENHANCED STRESS REDUCTION PACKAGE is a medical device that received FDA 510(k) clearance on 1991-01-25. The listed applicant is Bodylog, Inc.. The 510(k) number is K902450.

When did BODYLOG ENHANCED STRESS REDUCTION PACKAGE receive FDA 510(k) clearance?

BODYLOG ENHANCED STRESS REDUCTION PACKAGE received FDA 510(k) clearance on 1991-01-25, under 510(k) number K902450.

Who is the listed applicant for BODYLOG ENHANCED STRESS REDUCTION PACKAGE?

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

What is the FDA product code for BODYLOG ENHANCED STRESS REDUCTION PACKAGE?

The FDA product code for BODYLOG ENHANCED STRESS REDUCTION PACKAGE is HCC.

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 Bodylog, 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.

K873418BODYLOG STRESS REDUCTION PACKAGEK854208THE BODYLOG 500 RET THERAPEUTIC ELECTROMYOGRAPHICS

Related Devices (Code: HCC)

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.

K233580A Breathing System (ABS)Deepwell Dtx, Inc.K222101PrismGraymatters Health , Ltd.K180173FreespiraPalo Alto Health Sciences, Inc.K163448GrindCare SystemSunstar Suisse S.A.K131586CANARY BREATHING SYSTEMPalo Alto Health Sciences, Inc.K122879EEGER4 MODEL 4.3Eeg Software, LLC

Official Source

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