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FDA 510(k)

SYNEVAC VACUUM CURETTAGE SYSTEMS

K-Number: K813282 · 1981-12-14

ApplicantSynemed, Inc.
Decision Date1981-12-14
Product CodeHHI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SYNEVAC VACUUM CURETTAGE SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Synemed, Inc.. It received FDA 510(k) clearance on 1981-12-14 under 510(k) number K813282. 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 SYNEVAC VACUUM CURETTAGE SYSTEMS?

SYNEVAC VACUUM CURETTAGE SYSTEMS is a medical device that received FDA 510(k) clearance on 1981-12-14. The listed applicant is Synemed, Inc.. The 510(k) number is K813282.

When did SYNEVAC VACUUM CURETTAGE SYSTEMS receive FDA 510(k) clearance?

SYNEVAC VACUUM CURETTAGE SYSTEMS received FDA 510(k) clearance on 1981-12-14, under 510(k) number K813282.

Who is the listed applicant for SYNEVAC VACUUM CURETTAGE SYSTEMS?

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

What is the FDA product code for SYNEVAC VACUUM CURETTAGE SYSTEMS?

The FDA product code for SYNEVAC VACUUM CURETTAGE SYSTEMS is HHI.

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Other records listing Synemed, 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.

K954037FIELD TRENDK852936THE FIELDMASTER MODEL 275K833274DERMATOLOGY HANDPIECE-OPHTH LASERK831085SYNEVAC VACUUM SOURCE UNITK828585OPTHALAS PHOTOCOAGULATORK822853MODEL 200 SQUID

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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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