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FDA 510(k)

BAXTER D & C TRAY

K-Number: K901442 · 1990-07-26

ApplicantBaxter Healthcare Corp
Decision Date1990-07-26
Product CodeHCY
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

BAXTER D & C TRAY 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 1990-07-26 under 510(k) number K901442. The device is classified under product code HCY. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BAXTER D & C TRAY?

BAXTER D & C TRAY is a medical device that received FDA 510(k) clearance on 1990-07-26. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K901442.

When did BAXTER D & C TRAY receive FDA 510(k) clearance?

BAXTER D & C TRAY received FDA 510(k) clearance on 1990-07-26, under 510(k) number K901442.

Who is the listed applicant for BAXTER D & C TRAY?

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 BAXTER D & C TRAY?

The FDA product code for BAXTER D & C TRAY is HCY.

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Other records listing Baxter Healthcare Corp as applicant

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Related Devices (Code: HCY)

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.

K980096OAC (OPTICAL ASPIRATING CURETTE)Imagyn Medical Technologies, Inc.K944238ENDOCYTE TMD.L. Nelson and Assoc., Inc.K935822PHASE I CURETTEPhase I Corp.K890384UTERINE CURETTEKinetic Medical ProductsK881794IVORY FINDER SETIvory Instruments Co.K862297THE D & C PAD-SACNu-Gyn-Tek, 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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