LATEX FINGER COT, POWDER-FREE, WITH PROTEIN LABELING
K-Number: K980827 · 1998-05-04
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Device Summary
Frequently Asked Questions
What is the LATEX FINGER COT, POWDER-FREE, WITH PROTEIN LABELING?
LATEX FINGER COT, POWDER-FREE, WITH PROTEIN LABELING is a medical device that received FDA 510(k) clearance on 1998-05-04. The listed applicant is Tucker & Associates. The 510(k) number is K980827.
When did LATEX FINGER COT, POWDER-FREE, WITH PROTEIN LABELING receive FDA 510(k) clearance?
LATEX FINGER COT, POWDER-FREE, WITH PROTEIN LABELING received FDA 510(k) clearance on 1998-05-04, under 510(k) number K980827.
Who is the listed applicant for LATEX FINGER COT, POWDER-FREE, WITH PROTEIN LABELING?
The FDA 510(k) record lists Tucker & Associates as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATEX FINGER COT, POWDER-FREE, WITH PROTEIN LABELING?
The FDA product code for LATEX FINGER COT, POWDER-FREE, WITH PROTEIN LABELING is LZB.
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 Tucker & Associates 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: LZB)
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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