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FDA 510(k)

THERMO FORMA, CRYOMED, CONTROLLED RATE FREEZERS; MODELS # 7456, 7457, 7458,7459,7475,7476

K-Number: K021042 · 2002-05-15

ApplicantThermo Forma, Inc.
Decision Date2002-05-15
Product CodeMQG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

THERMO FORMA, CRYOMED, CONTROLLED RATE FREEZERS; MODELS # 7456, 7457, 7458,7459,7475,7476 is the device name listed in this FDA 510(k) record. The listed applicant is Thermo Forma, Inc.. It received FDA 510(k) clearance on 2002-05-15 under 510(k) number K021042. The device is classified under product code MQG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERMO FORMA, CRYOMED, CONTROLLED RATE FREEZERS; MODELS # 7456, 7457, 7458,7459,7475,7476?

THERMO FORMA, CRYOMED, CONTROLLED RATE FREEZERS; MODELS # 7456, 7457, 7458,7459,7475,7476 is a medical device that received FDA 510(k) clearance on 2002-05-15. The listed applicant is Thermo Forma, Inc.. The 510(k) number is K021042.

When did THERMO FORMA, CRYOMED, CONTROLLED RATE FREEZERS; MODELS # 7456, 7457, 7458,7459,7475,7476 receive FDA 510(k) clearance?

THERMO FORMA, CRYOMED, CONTROLLED RATE FREEZERS; MODELS # 7456, 7457, 7458,7459,7475,7476 received FDA 510(k) clearance on 2002-05-15, under 510(k) number K021042.

Who is the listed applicant for THERMO FORMA, CRYOMED, CONTROLLED RATE FREEZERS; MODELS # 7456, 7457, 7458,7459,7475,7476?

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

What is the FDA product code for THERMO FORMA, CRYOMED, CONTROLLED RATE FREEZERS; MODELS # 7456, 7457, 7458,7459,7475,7476?

The FDA product code for THERMO FORMA, CRYOMED, CONTROLLED RATE FREEZERS; MODELS # 7456, 7457, 7458,7459,7475,7476 is MQG.

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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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