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FDA 510(k)

BISSINGER CABLES, CAT. NO. 801000XX

K-Number: K981919 · 1998-08-06

ApplicantGuenter Bissinger Medizintechnik GmbH
Decision Date1998-08-06
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BISSINGER CABLES, CAT. NO. 801000XX is the device name listed in this FDA 510(k) record. The listed applicant is Guenter Bissinger Medizintechnik GmbH. It received FDA 510(k) clearance on 1998-08-06 under 510(k) number K981919. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BISSINGER CABLES, CAT. NO. 801000XX?

BISSINGER CABLES, CAT. NO. 801000XX is a medical device that received FDA 510(k) clearance on 1998-08-06. The listed applicant is Guenter Bissinger Medizintechnik GmbH. The 510(k) number is K981919.

When did BISSINGER CABLES, CAT. NO. 801000XX receive FDA 510(k) clearance?

BISSINGER CABLES, CAT. NO. 801000XX received FDA 510(k) clearance on 1998-08-06, under 510(k) number K981919.

Who is the listed applicant for BISSINGER CABLES, CAT. NO. 801000XX?

The FDA 510(k) record lists Guenter Bissinger Medizintechnik GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BISSINGER CABLES, CAT. NO. 801000XX?

The FDA product code for BISSINGER CABLES, CAT. NO. 801000XX is GEI.

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Other records listing Guenter Bissinger Medizintechnik GmbH as applicant

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Related Devices (Code: GEI)

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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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