FDA 510(k)

SPOROX II STERILIZING & DISINFECTING SOLUTION

K-Number: K990703 · 1999-03-30

Decision Date1999-03-30

Product CodeMED

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SPOROX II STERILIZING & DISINFECTING SOLUTION 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 1999-03-30 under 510(k) number K990703. 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 II STERILIZING & DISINFECTING SOLUTION?

SPOROX II STERILIZING & DISINFECTING SOLUTION is a medical device that received FDA 510(k) clearance on 1999-03-30. The listed applicant is Reckitt Benckiser, Inc.. The 510(k) number is K990703.

When did SPOROX II STERILIZING & DISINFECTING SOLUTION receive FDA 510(k) clearance?

SPOROX II STERILIZING & DISINFECTING SOLUTION received FDA 510(k) clearance on 1999-03-30, under 510(k) number K990703.

Who is the listed applicant for SPOROX II STERILIZING & DISINFECTING SOLUTION?

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 II STERILIZING & DISINFECTING SOLUTION?

The FDA product code for SPOROX II STERILIZING & DISINFECTING SOLUTION 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Reckitt Benckiser, Inc. as applicant

K970230SPOROX K963353LYSOL I.C. BRAND PHENOLIC DISINFECTANT CLEANER (EPA REG. NO. 675-46)

Related Devices (Code: MED)

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.