VINYL EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.)
K-Number: K891726 · 1989-05-12
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Device Summary
Frequently Asked Questions
What is the VINYL EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.)?
VINYL EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.) is a medical device that received FDA 510(k) clearance on 1989-05-12. The listed applicant is Baldur Systems Corp.. The 510(k) number is K891726.
When did VINYL EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.) receive FDA 510(k) clearance?
VINYL EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.) received FDA 510(k) clearance on 1989-05-12, under 510(k) number K891726.
Who is the listed applicant for VINYL EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.)?
The FDA 510(k) record lists Baldur Systems Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VINYL EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.)?
The FDA product code for VINYL EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.) is LYZ.
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 Baldur Systems 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.
Related Devices (Code: LYZ)
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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