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FDA 510(k)

VAPOPHENE

K-Number: K961289 · 1997-12-04

ApplicantGermiphene Corp.
Decision Date1997-12-04
Product CodeMED
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VAPOPHENE is the device name listed in this FDA 510(k) record. The listed applicant is Germiphene Corp.. It received FDA 510(k) clearance on 1997-12-04 under 510(k) number K961289. The device is classified under product code MED. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAPOPHENE?

VAPOPHENE is a medical device that received FDA 510(k) clearance on 1997-12-04. The listed applicant is Germiphene Corp.. The 510(k) number is K961289.

When did VAPOPHENE receive FDA 510(k) clearance?

VAPOPHENE received FDA 510(k) clearance on 1997-12-04, under 510(k) number K961289.

Who is the listed applicant for VAPOPHENE?

The FDA 510(k) record lists Germiphene Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VAPOPHENE?

The FDA product code for VAPOPHENE is MED.

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.

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Other records listing Germiphene 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.

K983847MODIFICATION OF: ODYSSEY I DENTAL WATER UNITK964796ODYSSEY I DENTAL WATER UNITK942851SMILE INTEGRATED PROPHYLAXIS PASTE RINGSK894933PERLIDENT

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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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