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FDA 510(k)

THE STRIPPER

K-Number: K993699 · 2000-05-16

ApplicantMid-Atlantic Diagnostics, Inc.
Decision Date2000-05-16
Product CodeMQH
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

THE STRIPPER is the device name listed in this FDA 510(k) record. The listed applicant is Mid-Atlantic Diagnostics, Inc.. It received FDA 510(k) clearance on 2000-05-16 under 510(k) number K993699. The device is classified under product code MQH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE STRIPPER?

THE STRIPPER is a medical device that received FDA 510(k) clearance on 2000-05-16. The listed applicant is Mid-Atlantic Diagnostics, Inc.. The 510(k) number is K993699.

When did THE STRIPPER receive FDA 510(k) clearance?

THE STRIPPER received FDA 510(k) clearance on 2000-05-16, under 510(k) number K993699.

Who is the listed applicant for THE STRIPPER?

The FDA 510(k) record lists Mid-Atlantic Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE STRIPPER?

The FDA product code for THE STRIPPER is MQH.

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Other records listing Mid-Atlantic Diagnostics, 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.

K100596CRYOPETTEK041435THE STRIPPER PGDK030525CUSTOM PRODUCTS IVF WORKSTATION TYPE WKST-24*36, WKST-24*48, WKST-24*60, WKST-24*72 AND WKST-24*72D PLUS ACCESSORIES

Related Devices (Code: MQH)

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.

K250838Denudation PipettesGuangzhou Pinzhi Medical Device Co., Ltd.K192146V-DENUPETVitromed GmbHK161275EZ-Tip Singles, EZ-Tip Vial of 20, EZ-GripResearch Instruments LimitedK152581LifeGlobal Micro TipsLife Global Group, LLCK151018Embryo Biopsy Pipette, Polar Body Biopsy Pipette, Testicular Sperm Extraction PipetteCook IncorporatedK102480INJECTION PIPETTE; HOLDING PIPETTE; BIOPSY PIPETTE; DENUDING PIPETTE; PARTIAL ZONA DISSECTION (PZD) PIPETTE; ASSISTED HAJieying Laboratory, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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