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FDA 510(k)

BALLET STERILE DISPOSABLE ELECTROLYSIS

K-Number: K883892 · 1988-10-20

Decision Date1988-10-20
Product CodeKCW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BALLET STERILE DISPOSABLE ELECTROLYSIS is the device name listed in this FDA 510(k) record. The listed applicant is Synoptic Products. It received FDA 510(k) clearance on 1988-10-20 under 510(k) number K883892. The device is classified under product code KCW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BALLET STERILE DISPOSABLE ELECTROLYSIS?

BALLET STERILE DISPOSABLE ELECTROLYSIS is a medical device that received FDA 510(k) clearance on 1988-10-20. The listed applicant is Synoptic Products. The 510(k) number is K883892.

When did BALLET STERILE DISPOSABLE ELECTROLYSIS receive FDA 510(k) clearance?

BALLET STERILE DISPOSABLE ELECTROLYSIS received FDA 510(k) clearance on 1988-10-20, under 510(k) number K883892.

Who is the listed applicant for BALLET STERILE DISPOSABLE ELECTROLYSIS?

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

What is the FDA product code for BALLET STERILE DISPOSABLE ELECTROLYSIS?

The FDA product code for BALLET STERILE DISPOSABLE ELECTROLYSIS is KCW.

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.

Related Devices (Code: KCW)

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.

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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