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FDA 510(k)

SELICOR, MODELS A100 & D100

K-Number: K020227 · 2002-07-30

ApplicantSelicor, Inc.
Decision Date2002-07-30
Product CodeIMJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SELICOR, MODELS A100 & D100 is the device name listed in this FDA 510(k) record. The listed applicant is Selicor, Inc.. It received FDA 510(k) clearance on 2002-07-30 under 510(k) number K020227. The device is classified under product code IMJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SELICOR, MODELS A100 & D100?

SELICOR, MODELS A100 & D100 is a medical device that received FDA 510(k) clearance on 2002-07-30. The listed applicant is Selicor, Inc.. The 510(k) number is K020227.

When did SELICOR, MODELS A100 & D100 receive FDA 510(k) clearance?

SELICOR, MODELS A100 & D100 received FDA 510(k) clearance on 2002-07-30, under 510(k) number K020227.

Who is the listed applicant for SELICOR, MODELS A100 & D100?

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

What is the FDA product code for SELICOR, MODELS A100 & D100?

The FDA product code for SELICOR, MODELS A100 & D100 is IMJ.

Related Clinical Trials

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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Other records listing Selicor, 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.

K030382SELITHERM, MODEL C100

Related Devices (Code: IMJ)

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.

K252963BTL-899TTBTL Industries, Inc.K250376ViVYViatherm Therapeutics, LLCK243112Curapuls 670Enraf-Nonius, B.V.K223620Reprieve by RegenesisTMRegenesis Biomedical, Inc.K182363BTL-703BTL Industries, Inc.K173300ViaTherm BOOSTViatherm Therapeutics, LLC

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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