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FDA 510(k)

SPOROX

K-Number: K970230 · 1997-10-29

ApplicantReckitt Benckiser, Inc.
Decision Date1997-10-29
Product CodeMED
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SPOROX is the device name listed in this FDA 510(k) record. The listed applicant is Reckitt Benckiser, Inc.. It received FDA 510(k) clearance on 1997-10-29 under 510(k) number K970230. 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 SPOROX?

SPOROX is a medical device that received FDA 510(k) clearance on 1997-10-29. The listed applicant is Reckitt Benckiser, Inc.. The 510(k) number is K970230.

When did SPOROX receive FDA 510(k) clearance?

SPOROX received FDA 510(k) clearance on 1997-10-29, under 510(k) number K970230.

Who is the listed applicant for SPOROX?

The FDA 510(k) record lists Reckitt Benckiser, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPOROX?

The FDA product code for SPOROX is MED.

Related Clinical Trials

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Other records listing Reckitt Benckiser, 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.

K990703SPOROX II STERILIZING & DISINFECTING SOLUTIONK963353LYSOL I.C. BRAND PHENOLIC DISINFECTANT CLEANER (EPA REG. NO. 675-46)

Related Devices (Code: MED)

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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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