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FDA 510(k)

SUPPORT PRODUCTS EXAMPLE PROSET CAST

K-Number: K830650 · 1983-07-07

ApplicantIsopedix Corp.
Decision Date1983-07-07
Product CodeITG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SUPPORT PRODUCTS EXAMPLE PROSET CAST is the device name listed in this FDA 510(k) record. The listed applicant is Isopedix Corp.. It received FDA 510(k) clearance on 1983-07-07 under 510(k) number K830650. The device is classified under product code ITG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPPORT PRODUCTS EXAMPLE PROSET CAST?

SUPPORT PRODUCTS EXAMPLE PROSET CAST is a medical device that received FDA 510(k) clearance on 1983-07-07. The listed applicant is Isopedix Corp.. The 510(k) number is K830650.

When did SUPPORT PRODUCTS EXAMPLE PROSET CAST receive FDA 510(k) clearance?

SUPPORT PRODUCTS EXAMPLE PROSET CAST received FDA 510(k) clearance on 1983-07-07, under 510(k) number K830650.

Who is the listed applicant for SUPPORT PRODUCTS EXAMPLE PROSET CAST?

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

What is the FDA product code for SUPPORT PRODUCTS EXAMPLE PROSET CAST?

The FDA product code for SUPPORT PRODUCTS EXAMPLE PROSET CAST is ITG.

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Related Devices (Code: ITG)

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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