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FDA 510(k)

THE CABOT MEDICAL INSUL-SHETH VAGINAL SPECULUM COV

K-Number: K930954 · 1994-06-30

ApplicantCabot Medical Corp.
Decision Date1994-06-30
Product CodeHIB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

THE CABOT MEDICAL INSUL-SHETH VAGINAL SPECULUM COV is the device name listed in this FDA 510(k) record. The listed applicant is Cabot Medical Corp.. It received FDA 510(k) clearance on 1994-06-30 under 510(k) number K930954. The device is classified under product code HIB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE CABOT MEDICAL INSUL-SHETH VAGINAL SPECULUM COV?

THE CABOT MEDICAL INSUL-SHETH VAGINAL SPECULUM COV is a medical device that received FDA 510(k) clearance on 1994-06-30. The listed applicant is Cabot Medical Corp.. The 510(k) number is K930954.

When did THE CABOT MEDICAL INSUL-SHETH VAGINAL SPECULUM COV receive FDA 510(k) clearance?

THE CABOT MEDICAL INSUL-SHETH VAGINAL SPECULUM COV received FDA 510(k) clearance on 1994-06-30, under 510(k) number K930954.

Who is the listed applicant for THE CABOT MEDICAL INSUL-SHETH VAGINAL SPECULUM COV?

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

What is the FDA product code for THE CABOT MEDICAL INSUL-SHETH VAGINAL SPECULUM COV?

The FDA product code for THE CABOT MEDICAL INSUL-SHETH VAGINAL SPECULUM COV is HIB.

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Other records listing Cabot Medical 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.

K960148CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENTK946109CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPSK951972CABOT MEDICAL ULTRA FLOW CYSTOURETHROSCOPE SYSTEM WITH OPERATING & DIAGNOSTIC SHEATHSK951714CABOT MEDICAL-SURGITEK ULTRAGOLD PLUS SIDE-FIRING UROLOGIC LASER FIBERK941743CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMPK9341153000 ELECTRONIC INSUFFLATOR MODIFICATION

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Related Devices (Code: HIB)

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.

K252208JFord Speculum Sleeve™Ford Medtech, LLCK130046CLEARSPEC SINGLE USE VAGINAL SPECULUMClearspec, LLCK120743SPECULUM, VAGINAL, NONMETALWelch Allyn, Inc.K110766KOLPLUX SYSTEMKolplast CI LtdaK092870NON-STERILE DISPOSABLE VAGINAL SPECULUMKunshan Deyi Plastic Co., Ltd.K091937OFFICE-SPEC DISPOSABLE SIDE-OPENING SPECULUMObp Corporation

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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