LANDSCAPE PATIENT EXAMINATION GLOVES
K-Number: K893049 · 1989-09-05
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Device Summary
Frequently Asked Questions
What is the LANDSCAPE PATIENT EXAMINATION GLOVES?
LANDSCAPE PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-09-05. The listed applicant is Pacific Intl. Economic & Technical, Inc. U.S.A.. The 510(k) number is K893049.
When did LANDSCAPE PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?
LANDSCAPE PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 1989-09-05, under 510(k) number K893049.
Who is the listed applicant for LANDSCAPE PATIENT EXAMINATION GLOVES?
The FDA 510(k) record lists Pacific Intl. Economic & Technical, Inc. U.S.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LANDSCAPE PATIENT EXAMINATION GLOVES?
The FDA product code for LANDSCAPE PATIENT EXAMINATION GLOVES 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.
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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