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FDA 510(k)

CANNULA AND GENERAL PURPOSE ASPIRATOR

K-Number: K873552 · 1987-11-25

ApplicantCosmedtech, Inc.
Decision Date1987-11-25
Product CodeHHI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CANNULA AND GENERAL PURPOSE ASPIRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Cosmedtech, Inc.. It received FDA 510(k) clearance on 1987-11-25 under 510(k) number K873552. The device is classified under product code HHI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANNULA AND GENERAL PURPOSE ASPIRATOR?

CANNULA AND GENERAL PURPOSE ASPIRATOR is a medical device that received FDA 510(k) clearance on 1987-11-25. The listed applicant is Cosmedtech, Inc.. The 510(k) number is K873552.

When did CANNULA AND GENERAL PURPOSE ASPIRATOR receive FDA 510(k) clearance?

CANNULA AND GENERAL PURPOSE ASPIRATOR received FDA 510(k) clearance on 1987-11-25, under 510(k) number K873552.

Who is the listed applicant for CANNULA AND GENERAL PURPOSE ASPIRATOR?

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

What is the FDA product code for CANNULA AND GENERAL PURPOSE ASPIRATOR?

The FDA product code for CANNULA AND GENERAL PURPOSE ASPIRATOR is HHI.

Related Clinical Trials

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.

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Other records listing Cosmedtech, 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.

K870574COSMEDTECH GENERAL ASPIRATORK870560COSMEDTECH CANNULA

Related Devices (Code: HHI)

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.

K171440Berkeley VC-10 Vacuum Curettage SystemGyrus AcmiK030935BERKELEY V-10 VACUUM CURETTAGE SYSTEMAcmi CorporationK983181CYTOPREPCytoprep Inc. Est.K931205MEDI VAC SPECIMEN COLLECTOR AND TRANSPORTERBaxter Healthcare CorpK904160CYTOSMEAR BRUSHBrooke Intl.K900641CANNULA, SUCTION UTERINEWilliams Specialty Products, 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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