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FDA 510(k)

BRUSH, SCRUB, OPERATING ROOM

K-Number: K823061 · 1982-11-05

ApplicantSeamless Hospital Products Co.
Decision Date1982-11-05
Product CodeGEC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BRUSH, SCRUB, OPERATING ROOM is the device name listed in this FDA 510(k) record. The listed applicant is Seamless Hospital Products Co.. It received FDA 510(k) clearance on 1982-11-05 under 510(k) number K823061. The device is classified under product code GEC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRUSH, SCRUB, OPERATING ROOM?

BRUSH, SCRUB, OPERATING ROOM is a medical device that received FDA 510(k) clearance on 1982-11-05. The listed applicant is Seamless Hospital Products Co.. The 510(k) number is K823061.

When did BRUSH, SCRUB, OPERATING ROOM receive FDA 510(k) clearance?

BRUSH, SCRUB, OPERATING ROOM received FDA 510(k) clearance on 1982-11-05, under 510(k) number K823061.

Who is the listed applicant for BRUSH, SCRUB, OPERATING ROOM?

The FDA 510(k) record lists Seamless Hospital Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BRUSH, SCRUB, OPERATING ROOM?

The FDA product code for BRUSH, SCRUB, OPERATING ROOM is GEC.

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Other records listing Seamless Hospital Products Co. 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.

K841769INTERMITTENT URETHRAL CATHETER TRAYK821134DC PACK TMK820490IV START TRAYK781127CONNECTING TUBE, CONDUCTIVE, SURG.

Related Devices (Code: GEC)

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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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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