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FDA 510(k)

UNIVIT PROBE

K-Number: K950287 · 1995-04-10

ApplicantMedical Instrument Development Laboratories, Inc.
Decision Date1995-04-10
Product CodeHKP
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

UNIVIT PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Instrument Development Laboratories, Inc.. It received FDA 510(k) clearance on 1995-04-10 under 510(k) number K950287. The device is classified under product code HKP. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIVIT PROBE?

UNIVIT PROBE is a medical device that received FDA 510(k) clearance on 1995-04-10. The listed applicant is Medical Instrument Development Laboratories, Inc.. The 510(k) number is K950287.

When did UNIVIT PROBE receive FDA 510(k) clearance?

UNIVIT PROBE received FDA 510(k) clearance on 1995-04-10, under 510(k) number K950287.

Who is the listed applicant for UNIVIT PROBE?

The FDA 510(k) record lists Medical Instrument Development Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNIVIT PROBE?

The FDA product code for UNIVIT PROBE is HKP.

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Other records listing Medical Instrument Development Laboratories, 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.

K102222ULTIMATE VIT ENHAMCER (UVE)K020911MID LABS AUTONOMOUS VIT ENHANCER (AVE)K992943VIT ENHANCERK971067DIGI-INJECTORK934600MICRODRIVEK932669SUPRA-VIT(TM)

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Related Devices (Code: HKP)

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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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