LATEX EXAM GLOVES(MFG: SHANG HAI RONGTONG LATEX)
K-Number: K893694 · 1989-08-10
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Device Summary
Frequently Asked Questions
What is the LATEX EXAM GLOVES(MFG: SHANG HAI RONGTONG LATEX)?
LATEX EXAM GLOVES(MFG: SHANG HAI RONGTONG LATEX) is a medical device that received FDA 510(k) clearance on 1989-08-10. The listed applicant is Sinochem (Usa), Inc.. The 510(k) number is K893694.
When did LATEX EXAM GLOVES(MFG: SHANG HAI RONGTONG LATEX) receive FDA 510(k) clearance?
LATEX EXAM GLOVES(MFG: SHANG HAI RONGTONG LATEX) received FDA 510(k) clearance on 1989-08-10, under 510(k) number K893694.
Who is the listed applicant for LATEX EXAM GLOVES(MFG: SHANG HAI RONGTONG LATEX)?
The FDA 510(k) record lists Sinochem (Usa), Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATEX EXAM GLOVES(MFG: SHANG HAI RONGTONG LATEX)?
The FDA product code for LATEX EXAM GLOVES(MFG: SHANG HAI RONGTONG LATEX) 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 Sinochem (Usa), 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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