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FDA 510(k)

BATES BLANKET

K-Number: K894433 · 1989-08-11

ApplicantJoe B. Bates, MD, FAAP
Decision Date1989-08-11
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BATES BLANKET is the device name listed in this FDA 510(k) record. The listed applicant is Joe B. Bates, MD, FAAP. It received FDA 510(k) clearance on 1989-08-11 under 510(k) number K894433. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BATES BLANKET?

BATES BLANKET is a medical device that received FDA 510(k) clearance on 1989-08-11. The listed applicant is Joe B. Bates, MD, FAAP. The 510(k) number is K894433.

When did BATES BLANKET receive FDA 510(k) clearance?

BATES BLANKET received FDA 510(k) clearance on 1989-08-11, under 510(k) number K894433.

Who is the listed applicant for BATES BLANKET?

The FDA 510(k) record lists Joe B. Bates, MD, FAAP as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BATES BLANKET?

The FDA product code for BATES BLANKET is KKX.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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