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FDA 510(k)

CONSTI-SSAGE VIBRATOR/MASSAGE

K-Number: K900674 · 1990-03-02

ApplicantBio-Tech Co.
Decision Date1990-03-02
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CONSTI-SSAGE VIBRATOR/MASSAGE is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Tech Co.. It received FDA 510(k) clearance on 1990-03-02 under 510(k) number K900674. 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 CONSTI-SSAGE VIBRATOR/MASSAGE?

CONSTI-SSAGE VIBRATOR/MASSAGE is a medical device that received FDA 510(k) clearance on 1990-03-02. The listed applicant is Bio-Tech Co.. The 510(k) number is K900674.

When did CONSTI-SSAGE VIBRATOR/MASSAGE receive FDA 510(k) clearance?

CONSTI-SSAGE VIBRATOR/MASSAGE received FDA 510(k) clearance on 1990-03-02, under 510(k) number K900674.

Who is the listed applicant for CONSTI-SSAGE VIBRATOR/MASSAGE?

The FDA 510(k) record lists Bio-Tech Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONSTI-SSAGE VIBRATOR/MASSAGE?

The FDA product code for CONSTI-SSAGE VIBRATOR/MASSAGE is ISA.

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 Bio-Tech Co. 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.

K922142FX-CABLELOK SYSTEM

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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