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FDA 510(k)

FLOW MED 311

K-Number: K820165 · 1982-02-01

ApplicantD.R.O. Medical, Inc.
Decision Date1982-02-01
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FLOW MED 311 is the device name listed in this FDA 510(k) record. The listed applicant is D.R.O. Medical, Inc.. It received FDA 510(k) clearance on 1982-02-01 under 510(k) number K820165. The device is classified under product code FMG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOW MED 311?

FLOW MED 311 is a medical device that received FDA 510(k) clearance on 1982-02-01. The listed applicant is D.R.O. Medical, Inc.. The 510(k) number is K820165.

When did FLOW MED 311 receive FDA 510(k) clearance?

FLOW MED 311 received FDA 510(k) clearance on 1982-02-01, under 510(k) number K820165.

Who is the listed applicant for FLOW MED 311?

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

What is the FDA product code for FLOW MED 311?

The FDA product code for FLOW MED 311 is FMG.

Other records listing D.R.O. Medical, 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.

K844820FLOW MED SK 140 BURETK801821FLOW MED 150K801179FLOW MED 160K801004FLOW MED 160

Related Devices (Code: FMG)

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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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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