FDA 510(k)

2000 MODULAR THIRTY-NINE

K-Number: K962763 · 1996-10-07

Decision Date1996-10-07

Product CodeFNL

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

2000 MODULAR THIRTY-NINE is the device name listed in this FDA 510(k) record. The listed applicant is Equi-Tron Mfg., Inc.. It received FDA 510(k) clearance on 1996-10-07 under 510(k) number K962763. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 2000 MODULAR THIRTY-NINE?

2000 MODULAR THIRTY-NINE is a medical device that received FDA 510(k) clearance on 1996-10-07. The listed applicant is Equi-Tron Mfg., Inc.. The 510(k) number is K962763.

When did 2000 MODULAR THIRTY-NINE receive FDA 510(k) clearance?

2000 MODULAR THIRTY-NINE received FDA 510(k) clearance on 1996-10-07, under 510(k) number K962763.

Who is the listed applicant for 2000 MODULAR THIRTY-NINE?

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

What is the FDA product code for 2000 MODULAR THIRTY-NINE?

The FDA product code for 2000 MODULAR THIRTY-NINE is FNL.

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Other records listing Equi-Tron Mfg., Inc. as applicant

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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.