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FDA 510(k)

MULTISURFACE ROLLER BOTTLE (M.S.R.B.)

K-Number: K880509 · 1988-04-01

ApplicantMotil Plastics , Ltd.
Decision Date1988-04-01
Product CodeKJC
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MULTISURFACE ROLLER BOTTLE (M.S.R.B.) is the device name listed in this FDA 510(k) record. The listed applicant is Motil Plastics , Ltd.. It received FDA 510(k) clearance on 1988-04-01 under 510(k) number K880509. The device is classified under product code KJC. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTISURFACE ROLLER BOTTLE (M.S.R.B.)?

MULTISURFACE ROLLER BOTTLE (M.S.R.B.) is a medical device that received FDA 510(k) clearance on 1988-04-01. The listed applicant is Motil Plastics , Ltd.. The 510(k) number is K880509.

When did MULTISURFACE ROLLER BOTTLE (M.S.R.B.) receive FDA 510(k) clearance?

MULTISURFACE ROLLER BOTTLE (M.S.R.B.) received FDA 510(k) clearance on 1988-04-01, under 510(k) number K880509.

Who is the listed applicant for MULTISURFACE ROLLER BOTTLE (M.S.R.B.)?

The FDA 510(k) record lists Motil Plastics , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTISURFACE ROLLER BOTTLE (M.S.R.B.)?

The FDA product code for MULTISURFACE ROLLER BOTTLE (M.S.R.B.) is KJC.

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

Related Devices (Code: KJC)

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.

K873137IN VITRO 2.5X ROLLER BOTTLEIn Vitro Scientific ProductsK791049SYNALON ROLLER BOTTLEDynatech Laboratories, Inc.

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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