FDA 510(k)

TES-TAPE

K-Number: K922207 · 1993-06-15

Decision Date1993-06-15

Product CodeCGA

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

TES-TAPE is the device name listed in this FDA 510(k) record. The listed applicant is Lilly Research Laboratories. It received FDA 510(k) clearance on 1993-06-15 under 510(k) number K922207. The device is classified under product code CGA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TES-TAPE?

TES-TAPE is a medical device that received FDA 510(k) clearance on 1993-06-15. The listed applicant is Lilly Research Laboratories. The 510(k) number is K922207.

When did TES-TAPE receive FDA 510(k) clearance?

TES-TAPE received FDA 510(k) clearance on 1993-06-15, under 510(k) number K922207.

Who is the listed applicant for TES-TAPE?

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

What is the FDA product code for TES-TAPE?

The FDA product code for TES-TAPE is CGA.

Other records listing Lilly Research Laboratories 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.

K822866MOXALACTAM

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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.