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FDA 510(k)

TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATOR

K-Number: K955018 · 1996-01-30

ApplicantInstrumentarium Corp.
Decision Date1996-01-30
Product CodeFFT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentarium Corp.. It received FDA 510(k) clearance on 1996-01-30 under 510(k) number K955018. The device is classified under product code FFT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATOR?

TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATOR is a medical device that received FDA 510(k) clearance on 1996-01-30. The listed applicant is Instrumentarium Corp.. The 510(k) number is K955018.

When did TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATOR receive FDA 510(k) clearance?

TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATOR received FDA 510(k) clearance on 1996-01-30, under 510(k) number K955018.

Who is the listed applicant for TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATOR?

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

What is the FDA product code for TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATOR?

The FDA product code for TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATOR is FFT.

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Other records listing Instrumentarium Corp. 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.

K022630MODIFICATION TO FOCUSK001729FOCUSK001439ORTHOCEPH OC100 DK992385ORTHOPANTOMOGRAPH OP100DK981641MAMMOGRAPHY X-RAY EQUIPMENT MODELS MGF101 AND MGF110, ALPHA III, ALPHA ST, ALPHA RT AND ALPHA IQK962638TONOCAP, TC-200 AND ACCESSORY CATHETERS

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Related Devices (Code: FFT)

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.

K102543BRAVO PH MONITORING SYSTEM AND ACCESSORIESGiven Imaging , Ltd.K013951SANDHILL SCIENTIFIC PEDIATEC PH PROBESandhill Scientific, Inc.K002028BRAVO PH MONITORING SYSTEMEndonetics, Inc.K961346PH ANALYSIS MODULESynectics-DantecK950087LOT 440Medical Instruments Corporation Mic AGK945069FLEXILOG 2000Oakfield Instruments, Ltd.

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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