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FDA 510(k)

UNSTERILE PATIENT EXAMINATION GLOVE

K-Number: K890627 · 1989-03-23

ApplicantAladan Corp.
Decision Date1989-03-23
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

UNSTERILE PATIENT EXAMINATION GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Aladan Corp.. It received FDA 510(k) clearance on 1989-03-23 under 510(k) number K890627. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNSTERILE PATIENT EXAMINATION GLOVE?

UNSTERILE PATIENT EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1989-03-23. The listed applicant is Aladan Corp.. The 510(k) number is K890627.

When did UNSTERILE PATIENT EXAMINATION GLOVE receive FDA 510(k) clearance?

UNSTERILE PATIENT EXAMINATION GLOVE received FDA 510(k) clearance on 1989-03-23, under 510(k) number K890627.

Who is the listed applicant for UNSTERILE PATIENT EXAMINATION GLOVE?

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

What is the FDA product code for UNSTERILE PATIENT EXAMINATION GLOVE?

The FDA product code for UNSTERILE PATIENT EXAMINATION GLOVE is LYY.

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.

Other records listing Aladan 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.

View all 18 devices →

Related Devices (Code: LYY)

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

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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