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FDA 510(k)

BK-A; BK-B; BK-IS SEALING CAP

K-Number: K970204 · 1997-04-29

Decision Date1997-04-29
Product CodeDTD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BK-A; BK-B; BK-IS SEALING CAP is the device name listed in this FDA 510(k) record. The listed applicant is Biotronik, Inc.. It received FDA 510(k) clearance on 1997-04-29 under 510(k) number K970204. The device is classified under product code DTD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BK-A; BK-B; BK-IS SEALING CAP?

BK-A; BK-B; BK-IS SEALING CAP is a medical device that received FDA 510(k) clearance on 1997-04-29. The listed applicant is Biotronik, Inc.. The 510(k) number is K970204.

When did BK-A; BK-B; BK-IS SEALING CAP receive FDA 510(k) clearance?

BK-A; BK-B; BK-IS SEALING CAP received FDA 510(k) clearance on 1997-04-29, under 510(k) number K970204.

Who is the listed applicant for BK-A; BK-B; BK-IS SEALING CAP?

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

What is the FDA product code for BK-A; BK-B; BK-IS SEALING CAP?

The FDA product code for BK-A; BK-B; BK-IS SEALING CAP is DTD.

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.

Other records listing Biotronik, Inc. 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.

View all 79 devices →

Related Devices (Code: DTD)

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

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