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FDA 510(k)

P51 ANGIOPLASTY PRESSURE TRANSDUCER

K-Number: K813331 · 1981-12-29

ApplicantKonigsberg Instruments, Inc.
Decision Date1981-12-29
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

P51 ANGIOPLASTY PRESSURE TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Konigsberg Instruments, Inc.. It received FDA 510(k) clearance on 1981-12-29 under 510(k) number K813331. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P51 ANGIOPLASTY PRESSURE TRANSDUCER?

P51 ANGIOPLASTY PRESSURE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1981-12-29. The listed applicant is Konigsberg Instruments, Inc.. The 510(k) number is K813331.

When did P51 ANGIOPLASTY PRESSURE TRANSDUCER receive FDA 510(k) clearance?

P51 ANGIOPLASTY PRESSURE TRANSDUCER received FDA 510(k) clearance on 1981-12-29, under 510(k) number K813331.

Who is the listed applicant for P51 ANGIOPLASTY PRESSURE TRANSDUCER?

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

What is the FDA product code for P51 ANGIOPLASTY PRESSURE TRANSDUCER?

The FDA product code for P51 ANGIOPLASTY PRESSURE TRANSDUCER is LIT.

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Other records listing Konigsberg Instruments, 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.

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Related Devices (Code: LIT)

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Official Source

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