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FDA 510(k)

NUCLEOTOME

K-Number: K844131 · 1984-11-29

ApplicantMedical Instrument Development Laboratories, Inc.
Decision Date1984-11-29
Product CodeHSZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NUCLEOTOME 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 1984-11-29 under 510(k) number K844131. The device is classified under product code HSZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUCLEOTOME?

NUCLEOTOME is a medical device that received FDA 510(k) clearance on 1984-11-29. The listed applicant is Medical Instrument Development Laboratories, Inc.. The 510(k) number is K844131.

When did NUCLEOTOME receive FDA 510(k) clearance?

NUCLEOTOME received FDA 510(k) clearance on 1984-11-29, under 510(k) number K844131.

Who is the listed applicant for NUCLEOTOME?

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 NUCLEOTOME?

The FDA product code for NUCLEOTOME is HSZ.

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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-INJECTORK950287UNIVIT PROBEK934600MICRODRIVE

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Related Devices (Code: HSZ)

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.

K991588EMS SWISS ORTHOCLAST(Ems Sa) Electro Medical SystemsK972860CURVTEK TSR SYSTEMBiolectron, Inc.K970345ALIGNMENT INSTRUMENTRichard Wolf Medical Instruments Corp.K955084ASPACH 65,000 (MODIFICATION)The Anspach Effort, Inc.K954080SODEM HIGH SPEED SYSTEMSodem Diffusion SAK944590ETHICON DRILL BIT AND DRILL GUIDEETHICON, Inc.

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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