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FDA 510(k)

EQUIPMENT/MATERIAL DECONTAMINATING KIT

K-Number: K911299 · 1991-04-08

ApplicantRohm and Haas Co.
Decision Date1991-04-08
Product CodeKIE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EQUIPMENT/MATERIAL DECONTAMINATING KIT is the device name listed in this FDA 510(k) record. The listed applicant is Rohm and Haas Co.. It received FDA 510(k) clearance on 1991-04-08 under 510(k) number K911299. The device is classified under product code KIE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EQUIPMENT/MATERIAL DECONTAMINATING KIT?

EQUIPMENT/MATERIAL DECONTAMINATING KIT is a medical device that received FDA 510(k) clearance on 1991-04-08. The listed applicant is Rohm and Haas Co.. The 510(k) number is K911299.

When did EQUIPMENT/MATERIAL DECONTAMINATING KIT receive FDA 510(k) clearance?

EQUIPMENT/MATERIAL DECONTAMINATING KIT received FDA 510(k) clearance on 1991-04-08, under 510(k) number K911299.

Who is the listed applicant for EQUIPMENT/MATERIAL DECONTAMINATING KIT?

The FDA 510(k) record lists Rohm and Haas Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EQUIPMENT/MATERIAL DECONTAMINATING KIT?

The FDA product code for EQUIPMENT/MATERIAL DECONTAMINATING KIT is KIE.

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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Rohm and Haas Co. 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.

K834435CROWN & BRIDGE RESINK822722CROWN S BRIDGE RESINK820456CROWN & BRIDGE RESIN FOR FABRICAT/DE

Related Devices (Code: KIE)

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.

K964588WATERS 515 HPLC PUMP (515)Waters CorporationK935666PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMPThe Perkin-Elmer Corp.K924347WATERS(TM) 996 PDAMillipore Corp.K914841CHROMATOGRAPHY CLINICAL USE 75JQRMillipore Corp.K862506THE WATERS MODEL 990 PHOTODIODE ARRAY DETECTORMillipore Corp.K844947EMIT ANCILLARY REAGENTSSyva Co.

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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