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FDA 510(k)

TENDER TEMP

K-Number: K951939 · 1995-09-01

Decision Date1995-09-01
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TENDER TEMP is the device name listed in this FDA 510(k) record. The listed applicant is Investech, Ltd.. It received FDA 510(k) clearance on 1995-09-01 under 510(k) number K951939. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TENDER TEMP?

TENDER TEMP is a medical device that received FDA 510(k) clearance on 1995-09-01. The listed applicant is Investech, Ltd.. The 510(k) number is K951939.

When did TENDER TEMP receive FDA 510(k) clearance?

TENDER TEMP received FDA 510(k) clearance on 1995-09-01, under 510(k) number K951939.

Who is the listed applicant for TENDER TEMP?

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

What is the FDA product code for TENDER TEMP?

The FDA product code for TENDER TEMP is FLL.

Related Clinical Trials

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.

Related Devices (Code: FLL)

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.

Official Source

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