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FDA 510(k)

MODEL 50-01-27

K-Number: K830490 · 1983-03-31

ApplicantWindsor Medical, Inc.
Decision Date1983-03-31
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL 50-01-27 is the device name listed in this FDA 510(k) record. The listed applicant is Windsor Medical, Inc.. It received FDA 510(k) clearance on 1983-03-31 under 510(k) number K830490. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 50-01-27?

MODEL 50-01-27 is a medical device that received FDA 510(k) clearance on 1983-03-31. The listed applicant is Windsor Medical, Inc.. The 510(k) number is K830490.

When did MODEL 50-01-27 receive FDA 510(k) clearance?

MODEL 50-01-27 received FDA 510(k) clearance on 1983-03-31, under 510(k) number K830490.

Who is the listed applicant for MODEL 50-01-27?

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

What is the FDA product code for MODEL 50-01-27?

The FDA product code for MODEL 50-01-27 is FRN.

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Other records listing Windsor 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.

K841481WINDSOR MEDICAL MODEL 50-00002K832606WINDSOR MEDICAL VARIOUS MODELSK832641WINDSOR MEDICAL MODEL 52K830657AMBULATORY MARK XI DRUG INFUSION DEV-K830656AMBULATORY MARK III INFUSION DEVICEK830544WINDSOR MEDICAL, INC. 50-01-028

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Related Devices (Code: FRN)

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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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