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FDA 510(k)

CARE IV BURN PAD, CATALOG #'S BP2334,BP3472

K-Number: K855160 · 1986-01-24

ApplicantHoward Associates, Inc.
Decision Date1986-01-24
Product Code
DecisionSubstantially Equivalent

Device Summary

CARE IV BURN PAD, CATALOG #'S BP2334,BP3472 is the device name listed in this FDA 510(k) record. The listed applicant is Howard Associates, Inc.. It received FDA 510(k) clearance on 1986-01-24 under 510(k) number K855160. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARE IV BURN PAD, CATALOG #'S BP2334,BP3472?

CARE IV BURN PAD, CATALOG #'S BP2334,BP3472 is a medical device that received FDA 510(k) clearance on 1986-01-24. The listed applicant is Howard Associates, Inc.. The 510(k) number is K855160.

When did CARE IV BURN PAD, CATALOG #'S BP2334,BP3472 receive FDA 510(k) clearance?

CARE IV BURN PAD, CATALOG #'S BP2334,BP3472 received FDA 510(k) clearance on 1986-01-24, under 510(k) number K855160.

Who is the listed applicant for CARE IV BURN PAD, CATALOG #'S BP2334,BP3472?

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

Related Clinical Trials

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Other records listing Howard Associates, 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.

K892085PATIENT EXAMINATION GLOVES (LATEX)K891174PATIENT EXAMINATION GLOVES (LATEX)

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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