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FDA 510(k)

ENDOCERVICAL ASPIRATOR

K-Number: K902242 · 1990-10-09

ApplicantInnovative Medical Products, Inc.
Decision Date1990-10-09
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 Innovative Medical Products, Inc.. It received FDA 510(k) clearance on 1990-10-09 under 510(k) number K902242. 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 1990-10-09. The listed applicant is Innovative Medical Products, Inc.. The 510(k) number is K902242.

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

ENDOCERVICAL ASPIRATOR received FDA 510(k) clearance on 1990-10-09, under 510(k) number K902242.

Who is the listed applicant for ENDOCERVICAL ASPIRATOR?

The FDA 510(k) record lists Innovative Medical Products, 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.

Related Clinical Trials

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Other records listing Innovative Medical Products, 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.

K914538UPH-2000 UNIVERSAL OXIMETRY PROBE HOLDER

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.K902032O. B. PACK IVCustomed, Inc.K902954OBER2 MONITOR, EYE MOVEMENT (OPHTHALMIC)Permobil AB

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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