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FDA 510(k)

WALLACH CC/BRUSH

K-Number: K896065 · 1990-01-04

ApplicantWallach Surgical Devices, Inc.
Decision Date1990-01-04
Product CodeHHT
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

WALLACH CC/BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Wallach Surgical Devices, Inc.. It received FDA 510(k) clearance on 1990-01-04 under 510(k) number K896065. The device is classified under product code HHT. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WALLACH CC/BRUSH?

WALLACH CC/BRUSH is a medical device that received FDA 510(k) clearance on 1990-01-04. The listed applicant is Wallach Surgical Devices, Inc.. The 510(k) number is K896065.

When did WALLACH CC/BRUSH receive FDA 510(k) clearance?

WALLACH CC/BRUSH received FDA 510(k) clearance on 1990-01-04, under 510(k) number K896065.

Who is the listed applicant for WALLACH CC/BRUSH?

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

What is the FDA product code for WALLACH CC/BRUSH?

The FDA product code for WALLACH CC/BRUSH is HHT.

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Other records listing Wallach Surgical Devices, 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.

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Related Devices (Code: HHT)

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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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