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FDA 510(k)

PROGENY IMAGING SOFTWARE, MODEL# 500-405 (6,7,8).

K-Number: K070664 · 2007-04-26

ApplicantProgeny, Inc.
Decision Date2007-04-26
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PROGENY IMAGING SOFTWARE, MODEL# 500-405 (6,7,8). is the device name listed in this FDA 510(k) record. The listed applicant is Progeny, Inc.. It received FDA 510(k) clearance on 2007-04-26 under 510(k) number K070664. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROGENY IMAGING SOFTWARE, MODEL# 500-405 (6,7,8).?

PROGENY IMAGING SOFTWARE, MODEL# 500-405 (6,7,8). is a medical device that received FDA 510(k) clearance on 2007-04-26. The listed applicant is Progeny, Inc.. The 510(k) number is K070664.

When did PROGENY IMAGING SOFTWARE, MODEL# 500-405 (6,7,8). receive FDA 510(k) clearance?

PROGENY IMAGING SOFTWARE, MODEL# 500-405 (6,7,8). received FDA 510(k) clearance on 2007-04-26, under 510(k) number K070664.

Who is the listed applicant for PROGENY IMAGING SOFTWARE, MODEL# 500-405 (6,7,8).?

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

What is the FDA product code for PROGENY IMAGING SOFTWARE, MODEL# 500-405 (6,7,8).?

The FDA product code for PROGENY IMAGING SOFTWARE, MODEL# 500-405 (6,7,8). is MUH.

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Other records listing Progeny, 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.

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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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