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FDA 510(k)

INTERPRO INT'L, INC. ISOLATION GOWN

K-Number: K874766 · 1987-12-10

ApplicantInterpro Intl., Inc.
Decision Date1987-12-10
Product CodeFYC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INTERPRO INT'L, INC. ISOLATION GOWN is the device name listed in this FDA 510(k) record. The listed applicant is Interpro Intl., Inc.. It received FDA 510(k) clearance on 1987-12-10 under 510(k) number K874766. The device is classified under product code FYC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERPRO INT'L, INC. ISOLATION GOWN?

INTERPRO INT'L, INC. ISOLATION GOWN is a medical device that received FDA 510(k) clearance on 1987-12-10. The listed applicant is Interpro Intl., Inc.. The 510(k) number is K874766.

When did INTERPRO INT'L, INC. ISOLATION GOWN receive FDA 510(k) clearance?

INTERPRO INT'L, INC. ISOLATION GOWN received FDA 510(k) clearance on 1987-12-10, under 510(k) number K874766.

Who is the listed applicant for INTERPRO INT'L, INC. ISOLATION GOWN?

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

What is the FDA product code for INTERPRO INT'L, INC. ISOLATION GOWN?

The FDA product code for INTERPRO INT'L, INC. ISOLATION GOWN is FYC.

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Other records listing Interpro Intl., Inc. as applicant

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Related Devices (Code: FYC)

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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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