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FDA 510(k)

MEDITEC LINK

K-Number: K981196 · 1998-06-17

ApplicantAesculap-Meditec North America
Decision Date1998-06-17
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MEDITEC LINK is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap-Meditec North America. It received FDA 510(k) clearance on 1998-06-17 under 510(k) number K981196. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDITEC LINK?

MEDITEC LINK is a medical device that received FDA 510(k) clearance on 1998-06-17. The listed applicant is Aesculap-Meditec North America. The 510(k) number is K981196.

When did MEDITEC LINK receive FDA 510(k) clearance?

MEDITEC LINK received FDA 510(k) clearance on 1998-06-17, under 510(k) number K981196.

Who is the listed applicant for MEDITEC LINK?

The FDA 510(k) record lists Aesculap-Meditec North America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDITEC LINK?

The FDA product code for MEDITEC LINK is HQF.

Related Clinical Trials

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Other records listing Aesculap-Meditec North America 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.

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Related Devices (Code: HQF)

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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