PROVIDONE-IODINE SWABSTICKS
K-Number: K830393 · 1983-04-06
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Device Summary
Frequently Asked Questions
What is the PROVIDONE-IODINE SWABSTICKS?
PROVIDONE-IODINE SWABSTICKS is a medical device that received FDA 510(k) clearance on 1983-04-06. The listed applicant is H & P Industries, Inc.. The 510(k) number is K830393.
When did PROVIDONE-IODINE SWABSTICKS receive FDA 510(k) clearance?
PROVIDONE-IODINE SWABSTICKS received FDA 510(k) clearance on 1983-04-06, under 510(k) number K830393.
Who is the listed applicant for PROVIDONE-IODINE SWABSTICKS?
The FDA 510(k) record lists H & P Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROVIDONE-IODINE SWABSTICKS?
The FDA product code for PROVIDONE-IODINE SWABSTICKS is GEC.
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 H & P Industries, 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: GEC)
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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