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FDA 510(k)

MEDLINE STERILE GAUZE SPONGES

K-Number: K930697 · 1993-06-24

ApplicantMedline Industries, Inc.
Decision Date1993-06-24
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDLINE STERILE GAUZE SPONGES is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1993-06-24 under 510(k) number K930697. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDLINE STERILE GAUZE SPONGES?

MEDLINE STERILE GAUZE SPONGES is a medical device that received FDA 510(k) clearance on 1993-06-24. The listed applicant is Medline Industries, Inc.. The 510(k) number is K930697.

When did MEDLINE STERILE GAUZE SPONGES receive FDA 510(k) clearance?

MEDLINE STERILE GAUZE SPONGES received FDA 510(k) clearance on 1993-06-24, under 510(k) number K930697.

Who is the listed applicant for MEDLINE STERILE GAUZE SPONGES?

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

What is the FDA product code for MEDLINE STERILE GAUZE SPONGES?

The FDA product code for MEDLINE STERILE GAUZE SPONGES is NAD.

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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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