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FDA 510(k)

MAX I

K-Number: K831763 · 1984-01-27

ApplicantTrade Max, Inc.
Decision Date1984-01-27
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MAX I is the device name listed in this FDA 510(k) record. The listed applicant is Trade Max, Inc.. It received FDA 510(k) clearance on 1984-01-27 under 510(k) number K831763. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAX I?

MAX I is a medical device that received FDA 510(k) clearance on 1984-01-27. The listed applicant is Trade Max, Inc.. The 510(k) number is K831763.

When did MAX I receive FDA 510(k) clearance?

MAX I received FDA 510(k) clearance on 1984-01-27, under 510(k) number K831763.

Who is the listed applicant for MAX I?

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

What is the FDA product code for MAX I?

The FDA product code for MAX I is DQD.

Related Devices (Code: DQD)

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.

K261494Smart Wireless Stethoscope (STEMO310);Smart Wireless Stethoscope (STEMO710);Smart Wireless Stethoscope (STEMO720);Smart Wireless Stethoscope (STEMO730)Shanghai Hulu Devices Co., Ltd.K261694CORE 300 Digital StethoscopeEko Health, Inc.K252915AiSteth®Ai Health Highway India Pvt., Ltd.K252089Tyto Stethoscope (G3)Tyto Care , Ltd.K252076Kneevoice Cartilage Evaluation System (750-3600-001)Kneevoice, Inc.K252284eMurmur Heart AICsd Labs

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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