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FDA 510(k)

IMPULS 3, IT SELECTOR

K-Number: K842805 · 1984-08-01

ApplicantRobert Bosch Corp.
Decision Date1984-08-01
Product CodeISB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

IMPULS 3, IT SELECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Robert Bosch Corp.. It received FDA 510(k) clearance on 1984-08-01 under 510(k) number K842805. The device is classified under product code ISB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPULS 3, IT SELECTOR?

IMPULS 3, IT SELECTOR is a medical device that received FDA 510(k) clearance on 1984-08-01. The listed applicant is Robert Bosch Corp.. The 510(k) number is K842805.

When did IMPULS 3, IT SELECTOR receive FDA 510(k) clearance?

IMPULS 3, IT SELECTOR received FDA 510(k) clearance on 1984-08-01, under 510(k) number K842805.

Who is the listed applicant for IMPULS 3, IT SELECTOR?

The FDA 510(k) record lists Robert Bosch Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMPULS 3, IT SELECTOR?

The FDA product code for IMPULS 3, IT SELECTOR is ISB.

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Other records listing Robert Bosch Corp. 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.

K854492ERG 551 ERGOMETER, BICYCLEK854493ERG 555 COUCH ERGOMETERK854491ERG 550 ERGOMETER BICYCLEK853154HV-4K853541SP 4K853271HEARING AID ANALYSIS SYSTEM

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Related Devices (Code: ISB)

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.

K842262PIRD-YPirdy, Inc.K790949GALVANIC UNITRami International Corp.K780632MAXICEPTORMed GeneralK780730FIGURETRIMJay-Mar INternational Enterprises, IN

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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