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FDA 510(k)

MEDLINES REPEAT PERFORMANCE SURGICAL PACK SYSTEM

K-Number: K930700 · 1993-07-09

ApplicantMedline Industries, Inc.
Decision Date1993-07-09
Product CodeLRO
Advisory CommitteeSU
DecisionUnknown

Device Summary

MEDLINES REPEAT PERFORMANCE SURGICAL PACK SYSTEM 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 1993-07-09 under 510(k) number K930700. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MEDLINES REPEAT PERFORMANCE SURGICAL PACK SYSTEM?

MEDLINES REPEAT PERFORMANCE SURGICAL PACK SYSTEM is a medical device that received FDA 510(k) clearance on 1993-07-09. The listed applicant is Medline Industries, Inc.. The 510(k) number is K930700.

When did MEDLINES REPEAT PERFORMANCE SURGICAL PACK SYSTEM receive FDA 510(k) clearance?

MEDLINES REPEAT PERFORMANCE SURGICAL PACK SYSTEM received FDA 510(k) clearance on 1993-07-09, under 510(k) number K930700.

Who is the listed applicant for MEDLINES REPEAT PERFORMANCE SURGICAL PACK SYSTEM?

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 MEDLINES REPEAT PERFORMANCE SURGICAL PACK SYSTEM?

The FDA product code for MEDLINES REPEAT PERFORMANCE SURGICAL PACK SYSTEM is LRO.

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Related Devices (Code: LRO)

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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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