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FDA 510(k)

BK-N SEALING CAP

K-Number: K971930 · 1997-08-14

ApplicantBiotronik, Inc.
Decision Date1997-08-14
Product CodeDTD
Advisory CommitteeCV
DecisionSubstantially Equivalent - Subject to Tracking & PMS

Device Summary

BK-N 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 1997-08-14 under 510(k) number K971930. The device is classified under product code DTD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking & PMS.

Frequently Asked Questions

What is the BK-N SEALING CAP?

BK-N SEALING CAP is a medical device that received FDA 510(k) clearance on 1997-08-14. The listed applicant is Biotronik, Inc.. The 510(k) number is K971930.

When did BK-N SEALING CAP receive FDA 510(k) clearance?

BK-N SEALING CAP received FDA 510(k) clearance on 1997-08-14, under 510(k) number K971930.

Who is the listed applicant for BK-N 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-N SEALING CAP?

The FDA product code for BK-N SEALING CAP is DTD.

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Other records listing Biotronik, Inc. as applicant

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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.

K1320086981M LEAD EXTENDER KIT, 6984M LEAD EXTENDER KIT, 6986M LEAD EXTENDER KIT, 5866-24M LEAD ADAPTOR KIT, 5866-38M LEAD ADAPMedtronic, Inc.K041574CPI LEAD ADAPTERS, MODELS 6017, 6018 AND 6020Guidant CorporationK031164PACING LEAD ADAPTORS, BIPOLAR, MODELS ILINK-BIS, ILINK-BLVOscor, Inc.K024156PACING LEAD EXTENSIONS, BIPOLAR, PACING LEAD ADAPTORS, UNIPOLAR/BIPOLAR,PACING LEAD ADAPTORS, UNIPOLAR/BIPOLAROscor, Inc.K010787PACING LEAD BIPOLAR ADAPTERS AND EXTENSIONSOscor, Inc.K003454A1-CS-SB Y-ADAPTER, MODEL 124 871Biotronik, Inc.

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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