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FDA 510(k)

VACOMED 4

K-Number: K842802 · 1984-08-01

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

Device Summary

VACOMED 4 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 K842802. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACOMED 4?

VACOMED 4 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 K842802.

When did VACOMED 4 receive FDA 510(k) clearance?

VACOMED 4 received FDA 510(k) clearance on 1984-08-01, under 510(k) number K842802.

Who is the listed applicant for VACOMED 4?

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 VACOMED 4?

The FDA product code for VACOMED 4 is ISA.

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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: ISA)

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.

K243488VMAT PROTermosaludK240358ShockPhysio Mobile (model SW3200 Basic)Shenzhen Dongdixin Technology Co., Ltd.K221865BTL-094BTL Industries, Inc.K210166Omnispec ED1000Medispec, Ltd.K213120OW100S (model OW100S-US)Tissue Regeneration Technologies, LLC Dba AS Softwave TrtK220538DolorClast RadialE.M.S Electro Medical Systems S.A

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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