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FDA 510(k)

PROBE SHEATH FOR ADMS & CAPISTRANO LABS TRANSREC.

K-Number: K896680 · 1990-02-14

ApplicantInterson Corp.
Decision Date1990-02-14
Product CodeFED
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PROBE SHEATH FOR ADMS & CAPISTRANO LABS TRANSREC. is the device name listed in this FDA 510(k) record. The listed applicant is Interson Corp.. It received FDA 510(k) clearance on 1990-02-14 under 510(k) number K896680. The device is classified under product code FED. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROBE SHEATH FOR ADMS & CAPISTRANO LABS TRANSREC.?

PROBE SHEATH FOR ADMS & CAPISTRANO LABS TRANSREC. is a medical device that received FDA 510(k) clearance on 1990-02-14. The listed applicant is Interson Corp.. The 510(k) number is K896680.

When did PROBE SHEATH FOR ADMS & CAPISTRANO LABS TRANSREC. receive FDA 510(k) clearance?

PROBE SHEATH FOR ADMS & CAPISTRANO LABS TRANSREC. received FDA 510(k) clearance on 1990-02-14, under 510(k) number K896680.

Who is the listed applicant for PROBE SHEATH FOR ADMS & CAPISTRANO LABS TRANSREC.?

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

What is the FDA product code for PROBE SHEATH FOR ADMS & CAPISTRANO LABS TRANSREC.?

The FDA product code for PROBE SHEATH FOR ADMS & CAPISTRANO LABS TRANSREC. is FED.

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Other records listing Interson Corp. as applicant

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Related Devices (Code: FED)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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