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FDA 510(k)

ENDOCERVICAL ASPIRATOR

K-Number: K812175 · 1981-09-21

ApplicantFertility Instrumentation, Inc.
Decision Date1981-09-21
Product CodeHFC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ENDOCERVICAL ASPIRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Fertility Instrumentation, Inc.. It received FDA 510(k) clearance on 1981-09-21 under 510(k) number K812175. The device is classified under product code HFC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOCERVICAL ASPIRATOR?

ENDOCERVICAL ASPIRATOR is a medical device that received FDA 510(k) clearance on 1981-09-21. The listed applicant is Fertility Instrumentation, Inc.. The 510(k) number is K812175.

When did ENDOCERVICAL ASPIRATOR receive FDA 510(k) clearance?

ENDOCERVICAL ASPIRATOR received FDA 510(k) clearance on 1981-09-21, under 510(k) number K812175.

Who is the listed applicant for ENDOCERVICAL ASPIRATOR?

The FDA 510(k) record lists Fertility Instrumentation, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOCERVICAL ASPIRATOR?

The FDA product code for ENDOCERVICAL ASPIRATOR is HFC.

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Related Devices (Code: HFC)

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.

K974032ROCKET MUCUS SAMPLER SYRINGE, STERILE, ROCKET MUCUS SAMPLER SYRINGE, CLINICALLY ASPIRATORA & A Medical, Inc.K960263CERVICAL MUCOUS ASPIRATION CATHETERCook Urological, Inc.K954903PEDI VAGINAL ASPIRATORCook Urological, Inc.K954102SELECTMUCUSSelect Medical Systems, Inc.K902242ENDOCERVICAL ASPIRATORInnovative Medical Products, Inc.K902032O. B. PACK IVCustomed, 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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