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FDA 510(k)

ELECTRO-SAGE MODEL 203

K-Number: K842379 · 1984-08-10

ApplicantWeingart, Inc.
Decision Date1984-08-10
Product CodeIRO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ELECTRO-SAGE MODEL 203 is the device name listed in this FDA 510(k) record. The listed applicant is Weingart, Inc.. It received FDA 510(k) clearance on 1984-08-10 under 510(k) number K842379. The device is classified under product code IRO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRO-SAGE MODEL 203?

ELECTRO-SAGE MODEL 203 is a medical device that received FDA 510(k) clearance on 1984-08-10. The listed applicant is Weingart, Inc.. The 510(k) number is K842379.

When did ELECTRO-SAGE MODEL 203 receive FDA 510(k) clearance?

ELECTRO-SAGE MODEL 203 received FDA 510(k) clearance on 1984-08-10, under 510(k) number K842379.

Who is the listed applicant for ELECTRO-SAGE MODEL 203?

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

What is the FDA product code for ELECTRO-SAGE MODEL 203?

The FDA product code for ELECTRO-SAGE MODEL 203 is IRO.

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 Weingart, 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.

K863518WEINGART MODEL 1000 SUNLAMP PRODUCTK842975BROWNIE BOOTH BB1

Related Devices (Code: IRO)

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.

K955160COMFORT, MUSCLE, CORDLESS MASSAGER, BATTERY POWERED OPERATED MASSAGEREverapex Design & Marketing Corp.K955250QI GONG MASSAGEREast Health Development Group, Inc.K954203MASSAGER THERAPUTIC, ELECTRICCisco Sales Corp.K952916SHIATSU MASTER MASSAGER CUSHIONKinsei Shiatsu, Inc.K951414CHAMPION PHYSIOACOUSTICC RECLINER-TRANSPORTER CHAIRChampion Mfg. Corp.K950441CONAIR FAMILY FITNESS BODY ENERGYConair 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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