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FDA 510(k)

CYMED MICROSKIN(R) DISPOSABLE IRRIGATION SLEEVE

K-Number: K892521 · 1989-05-01

ApplicantCymed, Inc.
Decision Date1989-05-01
Product CodeFZS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CYMED MICROSKIN(R) DISPOSABLE IRRIGATION SLEEVE is the device name listed in this FDA 510(k) record. The listed applicant is Cymed, Inc.. It received FDA 510(k) clearance on 1989-05-01 under 510(k) number K892521. The device is classified under product code FZS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYMED MICROSKIN(R) DISPOSABLE IRRIGATION SLEEVE?

CYMED MICROSKIN(R) DISPOSABLE IRRIGATION SLEEVE is a medical device that received FDA 510(k) clearance on 1989-05-01. The listed applicant is Cymed, Inc.. The 510(k) number is K892521.

When did CYMED MICROSKIN(R) DISPOSABLE IRRIGATION SLEEVE receive FDA 510(k) clearance?

CYMED MICROSKIN(R) DISPOSABLE IRRIGATION SLEEVE received FDA 510(k) clearance on 1989-05-01, under 510(k) number K892521.

Who is the listed applicant for CYMED MICROSKIN(R) DISPOSABLE IRRIGATION SLEEVE?

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

What is the FDA product code for CYMED MICROSKIN(R) DISPOSABLE IRRIGATION SLEEVE?

The FDA product code for CYMED MICROSKIN(R) DISPOSABLE IRRIGATION SLEEVE is FZS.

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Related Devices (Code: FZS)

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.

K932493SURGICAL CURETTEWhitney Products, Inc.K902000KEVTEK(TM) LASER DRAPE/ORGAN PROTECTOR/EYE SHIELDKevtek Medical Products, Inc.K891888CURRETTES - PIFFARD, WOLF, VIDAL-SCRAPERZinnanti Surgical Instruments, Inc.K891334ACU-CURETTEAcuderm, Inc.K890366ADENOID CURETTEKinetic Medical ProductsK875292MICRODISCECTOMY CURETTE SETT. Korossurgical Instruments Corp.

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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