FDA 510(k)

LOT 440

K-Number: K950087 · 1996-02-06

ApplicantMedical Instruments Corporation Mic AG

Decision Date1996-02-06

Product CodeFFT

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

LOT 440 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Instruments Corporation Mic AG. It received FDA 510(k) clearance on 1996-02-06 under 510(k) number K950087. 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 LOT 440?

LOT 440 is a medical device that received FDA 510(k) clearance on 1996-02-06. The listed applicant is Medical Instruments Corporation Mic AG. The 510(k) number is K950087.

When did LOT 440 receive FDA 510(k) clearance?

LOT 440 received FDA 510(k) clearance on 1996-02-06, under 510(k) number K950087.

Who is the listed applicant for LOT 440?

The FDA 510(k) record lists Medical Instruments Corporation Mic AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOT 440?

The FDA product code for LOT 440 is FFT.

Other records listing Medical Instruments Corporation Mic AG 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.

K991248PRONTO DRY

Related Devices (Code: FFT)

K102543BRAVO PH MONITORING SYSTEM AND ACCESSORIESGiven Imaging , Ltd.K013951SANDHILL SCIENTIFIC PEDIATEC PH PROBESandhill Scientific, Inc.K002028BRAVO PH MONITORING SYSTEMEndonetics, Inc.K961346PH ANALYSIS MODULESynectics-Dantec K955018TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATORInstrumentarium Corp.K945069FLEXILOG 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.