FDA 510(k)

IPG-300

K-Number: K852238 · 1985-10-11

Decision Date1985-10-11

Product CodeDSB

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

IPG-300 is the device name listed in this FDA 510(k) record. The listed applicant is Thornton Associates, Inc.. It received FDA 510(k) clearance on 1985-10-11 under 510(k) number K852238. The device is classified under product code DSB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IPG-300?

IPG-300 is a medical device that received FDA 510(k) clearance on 1985-10-11. The listed applicant is Thornton Associates, Inc.. The 510(k) number is K852238.

When did IPG-300 receive FDA 510(k) clearance?

IPG-300 received FDA 510(k) clearance on 1985-10-11, under 510(k) number K852238.

Who is the listed applicant for IPG-300?

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

What is the FDA product code for IPG-300?

The FDA product code for IPG-300 is DSB.

Other records listing Thornton Associates, 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.

K920514SPIRAL

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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.