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FDA 510(k)

PROVIDONE-IODINE SWABSTICKS

K-Number: K830393 · 1983-04-06

Decision Date1983-04-06
Product CodeGEC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PROVIDONE-IODINE SWABSTICKS is the device name listed in this FDA 510(k) record. The listed applicant is H & P Industries, Inc.. It received FDA 510(k) clearance on 1983-04-06 under 510(k) number K830393. The device is classified under product code GEC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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