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FDA 510(k)

MASTER I

K-Number: K822696 · 1982-09-22

ApplicantMaster Medical Services, Inc.
Decision Date1982-09-22
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MASTER I is the device name listed in this FDA 510(k) record. The listed applicant is Master Medical Services, Inc.. It received FDA 510(k) clearance on 1982-09-22 under 510(k) number K822696. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASTER I?

MASTER I is a medical device that received FDA 510(k) clearance on 1982-09-22. The listed applicant is Master Medical Services, Inc.. The 510(k) number is K822696.

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

MASTER I received FDA 510(k) clearance on 1982-09-22, under 510(k) number K822696.

Who is the listed applicant for MASTER I?

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

What is the FDA product code for MASTER I?

The FDA product code for MASTER I is INI.

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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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