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FDA 510(k)

DISPOSABLE IV INDUCTION COVER

K-Number: K894427 · 1989-09-11

ApplicantCentral Plastic, Inc.
Decision Date1989-09-11
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE IV INDUCTION COVER is the device name listed in this FDA 510(k) record. The listed applicant is Central Plastic, Inc.. It received FDA 510(k) clearance on 1989-09-11 under 510(k) number K894427. The device is classified under product code FMK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE IV INDUCTION COVER?

DISPOSABLE IV INDUCTION COVER is a medical device that received FDA 510(k) clearance on 1989-09-11. The listed applicant is Central Plastic, Inc.. The 510(k) number is K894427.

When did DISPOSABLE IV INDUCTION COVER receive FDA 510(k) clearance?

DISPOSABLE IV INDUCTION COVER received FDA 510(k) clearance on 1989-09-11, under 510(k) number K894427.

Who is the listed applicant for DISPOSABLE IV INDUCTION COVER?

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

What is the FDA product code for DISPOSABLE IV INDUCTION COVER?

The FDA product code for DISPOSABLE IV INDUCTION COVER is FMK.

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 Central Plastic, 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.

K910104ANTI-FOG DISPOSABLE IV INDUCTION COVER

Related Devices (Code: FMK)

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.

K262526Safety lancet (XL)Tianjin Huahong Technology Co., Ltd.K261045Verifine Safety LancetsPromisemed Hangzhou Meditech Co., Ltd.K260191Safety lancet (XXXVII)Tianjin Huahong Technology Co., Ltd.K253605Safety Heel LancetNingbo Medsun Medical Co., Ltd.K252490Heel Stick Safety Lancet (HHZ-II, HHZ-III, HHZ-IV)Tianjin Huahong Technology Co., Ltd.K251694safety lancetTianjin Huahong Technology Co., 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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