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FDA 510(k)

SEAL-AWAY HEMOSTASIS ADAPTER, MODEL 406229

K-Number: K984062 · 1999-03-24

ApplicantDiag Corp.
Decision Date1999-03-24
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SEAL-AWAY HEMOSTASIS ADAPTER, MODEL 406229 is the device name listed in this FDA 510(k) record. The listed applicant is Diag Corp.. It received FDA 510(k) clearance on 1999-03-24 under 510(k) number K984062. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEAL-AWAY HEMOSTASIS ADAPTER, MODEL 406229?

SEAL-AWAY HEMOSTASIS ADAPTER, MODEL 406229 is a medical device that received FDA 510(k) clearance on 1999-03-24. The listed applicant is Diag Corp.. The 510(k) number is K984062.

When did SEAL-AWAY HEMOSTASIS ADAPTER, MODEL 406229 receive FDA 510(k) clearance?

SEAL-AWAY HEMOSTASIS ADAPTER, MODEL 406229 received FDA 510(k) clearance on 1999-03-24, under 510(k) number K984062.

Who is the listed applicant for SEAL-AWAY HEMOSTASIS ADAPTER, MODEL 406229?

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

What is the FDA product code for SEAL-AWAY HEMOSTASIS ADAPTER, MODEL 406229?

The FDA product code for SEAL-AWAY HEMOSTASIS ADAPTER, MODEL 406229 is DYB.

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Related Devices (Code: DYB)

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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