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FDA 510(k)

ANTI-FOG DISPOSABLE IV INDUCTION COVER

K-Number: K910104 · 1991-04-12

ApplicantCentral Plastic, Inc.
Decision Date1991-04-12
Product CodeEYF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ANTI-FOG 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 1991-04-12 under 510(k) number K910104. The device is classified under product code EYF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTI-FOG DISPOSABLE IV INDUCTION COVER?

ANTI-FOG DISPOSABLE IV INDUCTION COVER is a medical device that received FDA 510(k) clearance on 1991-04-12. The listed applicant is Central Plastic, Inc.. The 510(k) number is K910104.

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

ANTI-FOG DISPOSABLE IV INDUCTION COVER received FDA 510(k) clearance on 1991-04-12, under 510(k) number K910104.

Who is the listed applicant for ANTI-FOG 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 ANTI-FOG DISPOSABLE IV INDUCTION COVER?

The FDA product code for ANTI-FOG DISPOSABLE IV INDUCTION COVER is EYF.

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.

K894427DISPOSABLE IV INDUCTION COVER

Related Devices (Code: EYF)

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.

K922785IRRIVAGEAutovageK911407HARDING STERNAL SHIELDHarding Medical DevicesK904389SI-PRODavid F. TrungaleK832908COMFEEL PROTECTIVE RINGSColoplast A/S

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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