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FDA 510(k)

CYSTO APRONS IN VARIOUS SIZES

K-Number: K893842 · 1989-08-02

ApplicantBemiss Jason Corp.
Decision Date1989-08-02
Product CodeLYU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CYSTO APRONS IN VARIOUS SIZES is the device name listed in this FDA 510(k) record. The listed applicant is Bemiss Jason Corp.. It received FDA 510(k) clearance on 1989-08-02 under 510(k) number K893842. The device is classified under product code LYU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYSTO APRONS IN VARIOUS SIZES?

CYSTO APRONS IN VARIOUS SIZES is a medical device that received FDA 510(k) clearance on 1989-08-02. The listed applicant is Bemiss Jason Corp.. The 510(k) number is K893842.

When did CYSTO APRONS IN VARIOUS SIZES receive FDA 510(k) clearance?

CYSTO APRONS IN VARIOUS SIZES received FDA 510(k) clearance on 1989-08-02, under 510(k) number K893842.

Who is the listed applicant for CYSTO APRONS IN VARIOUS SIZES?

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

What is the FDA product code for CYSTO APRONS IN VARIOUS SIZES?

The FDA product code for CYSTO APRONS IN VARIOUS SIZES is LYU.

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Related Devices (Code: LYU)

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.

K011755STRYKER T4 HYTREL (R) TOGASStryker Corp.K965237NURSES BOUFFANT CAPCopioumed Intl., Inc.K970988FAR-EAST BOUFFANT CAPSFar East Science & Technology Development Co., Ltd.K964364DISPOSABLE APRONInstrument Makar, Inc.K961791DEPUY DISPOSABLE FILTER/HOODDepuy, Inc.K961454AMMI MAGNI-GUARDAmerican Medical Mfg., Inc.

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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