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FDA 510(k)

RINN E-Z CAPPER

K-Number: K913885 · 1991-12-13

ApplicantRinn Corp.
Decision Date1991-12-13
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RINN E-Z CAPPER is the device name listed in this FDA 510(k) record. The listed applicant is Rinn Corp.. It received FDA 510(k) clearance on 1991-12-13 under 510(k) number K913885. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RINN E-Z CAPPER?

RINN E-Z CAPPER is a medical device that received FDA 510(k) clearance on 1991-12-13. The listed applicant is Rinn Corp.. The 510(k) number is K913885.

When did RINN E-Z CAPPER receive FDA 510(k) clearance?

RINN E-Z CAPPER received FDA 510(k) clearance on 1991-12-13, under 510(k) number K913885.

Who is the listed applicant for RINN E-Z CAPPER?

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

What is the FDA product code for RINN E-Z CAPPER?

The FDA product code for RINN E-Z CAPPER is FMI.

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 Rinn 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.

K932134RINN UNIVERSAL COLLIMATORK828605BEAM LIMITING DEVICEK813378UNI-BITE DENTAL X-RAY FILM HOLDERK772313X-RAY CO-ORDINATOR

Related Devices (Code: FMI)

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.

K261266MOWANA™ Auto DuoPENTAMASTER MEDIQ SDN BHDK261719Promisemed X-Safety Pen NeedlePromisemed Hangzhou Meditech Co., Ltd.K262427Pen Needle (Ordinary Type I, Safety Type IIA, Safety Type IIB, Safety Type IIIA, Safety Type IIIB, Safety Type IV, Safety Type V, Ordinary Type VIA, Ordinary Type VIB, Ordinary Type VIC, Safety Type VII, Ordinary Type IB, Safety type VIII, Safety Type IX, Safety Type X, Ordinary Type XI, Safety Type XII)Hh Global Technology, Inc.K260933Safety Sterile Hypodermic Needles (NR-S1816R, NR-S1916R, NR-S1925R, NR-S1938R, NR-S2016R, NR-S2025R, NR-S2038R, NR-S2051R, NR-S2116R, NR-S2125R, NR-S2138R, NR-S2151R, NR-S2216R, NR-S2225R, NR-S2238R, NR-S2251R, NR-S2316R, NR-S2325R, NR-S2338R, NR-S2351R, NR-S2516R, NR-S2525R, NR-S2538R, NR-S2551R, NR-S2516T, NR-S2525T, NR-S2538T, NR-S2551T)Hangzhou Qiantang Longyue Biotechnology Co., Ltd.K261829Profoject™ Dual-Safety Pen NeedlesCMT Health PTE., Ltd.K260739Profoject™ Pen Needles (Model A; Model B)CMT Health PTE., Ltd.

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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