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FDA 510(k)

MEDDRAINS

K-Number: K931607 · 1993-08-06

ApplicantArmm, Inc.
Decision Date1993-08-06
Product CodeGBN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDDRAINS is the device name listed in this FDA 510(k) record. The listed applicant is Armm, Inc.. It received FDA 510(k) clearance on 1993-08-06 under 510(k) number K931607. The device is classified under product code GBN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDDRAINS?

MEDDRAINS is a medical device that received FDA 510(k) clearance on 1993-08-06. The listed applicant is Armm, Inc.. The 510(k) number is K931607.

When did MEDDRAINS receive FDA 510(k) clearance?

MEDDRAINS received FDA 510(k) clearance on 1993-08-06, under 510(k) number K931607.

Who is the listed applicant for MEDDRAINS?

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

What is the FDA product code for MEDDRAINS?

The FDA product code for MEDDRAINS is GBN.

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Other records listing Armm, 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.

K981286SUPERFLOW IRRIGATION AND ASPIRATION TUBING SETSK923201ENDOSI SUCTION IRRIGATORK922245SUPER-FLOW TUBING

Related Devices (Code: GBN)

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.

K802783SURGEONS CHOICE STAPLE, REMOVE/IMPLANTHospital Products Intl.

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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