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FDA 510(k)

MEDI VAC SPECIMEN COLLECTOR AND TRANSPORTER

K-Number: K931205 · 1994-03-15

ApplicantBaxter Healthcare Corp
Decision Date1994-03-15
Product CodeHHI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MEDI VAC SPECIMEN COLLECTOR AND TRANSPORTER is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1994-03-15 under 510(k) number K931205. 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 MEDI VAC SPECIMEN COLLECTOR AND TRANSPORTER?

MEDI VAC SPECIMEN COLLECTOR AND TRANSPORTER is a medical device that received FDA 510(k) clearance on 1994-03-15. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K931205.

When did MEDI VAC SPECIMEN COLLECTOR AND TRANSPORTER receive FDA 510(k) clearance?

MEDI VAC SPECIMEN COLLECTOR AND TRANSPORTER received FDA 510(k) clearance on 1994-03-15, under 510(k) number K931205.

Who is the listed applicant for MEDI VAC SPECIMEN COLLECTOR AND TRANSPORTER?

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

What is the FDA product code for MEDI VAC SPECIMEN COLLECTOR AND TRANSPORTER?

The FDA product code for MEDI VAC SPECIMEN COLLECTOR AND TRANSPORTER is HHI.

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Other records listing Baxter Healthcare Corp as applicant

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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.K904160CYTOSMEAR BRUSHBrooke Intl.K900641CANNULA, SUCTION UTERINEWilliams Specialty Products, Inc.K900642SWIVEL ADAPTERWilliams 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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