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FDA 510(k)

BAXTER DISPOSABLE CIRCUMCISION TRAY

K-Number: K884290 · 1988-12-08

ApplicantBaxter Healthcare Corp
Decision Date1988-12-08
Product CodeHFX
Advisory CommitteeOB
DecisionUnknown

Device Summary

BAXTER DISPOSABLE CIRCUMCISION 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 1988-12-08 under 510(k) number K884290. The device is classified under product code HFX. It was reviewed by the OB advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the BAXTER DISPOSABLE CIRCUMCISION TRAY?

BAXTER DISPOSABLE CIRCUMCISION TRAY is a medical device that received FDA 510(k) clearance on 1988-12-08. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K884290.

When did BAXTER DISPOSABLE CIRCUMCISION TRAY receive FDA 510(k) clearance?

BAXTER DISPOSABLE CIRCUMCISION TRAY received FDA 510(k) clearance on 1988-12-08, under 510(k) number K884290.

Who is the listed applicant for BAXTER DISPOSABLE CIRCUMCISION 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 DISPOSABLE CIRCUMCISION TRAY?

The FDA product code for BAXTER DISPOSABLE CIRCUMCISION TRAY is HFX.

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Related Devices (Code: HFX)

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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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