LATEX EXAMINATION GLOVES (MFG. NINGBO MEDICAL)
K-Number: K890891 · 1989-07-14
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Device Summary
Frequently Asked Questions
What is the LATEX EXAMINATION GLOVES (MFG. NINGBO MEDICAL)?
LATEX EXAMINATION GLOVES (MFG. NINGBO MEDICAL) is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is Interpro Intl., Inc.. The 510(k) number is K890891.
When did LATEX EXAMINATION GLOVES (MFG. NINGBO MEDICAL) receive FDA 510(k) clearance?
LATEX EXAMINATION GLOVES (MFG. NINGBO MEDICAL) received FDA 510(k) clearance on 1989-07-14, under 510(k) number K890891.
Who is the listed applicant for LATEX EXAMINATION GLOVES (MFG. NINGBO MEDICAL)?
The FDA 510(k) record lists Interpro Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATEX EXAMINATION GLOVES (MFG. NINGBO MEDICAL)?
The FDA product code for LATEX EXAMINATION GLOVES (MFG. NINGBO MEDICAL) 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 Interpro Intl., Inc. 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.
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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