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FDA 510(k)

PHARMASEAL SCRUB CARE-SURGICAL SCRUB BRUSH SPONGES

K-Number: K854232 · 1985-12-10

ApplicantAmerican Pharmaseal Div. Ahsc
Decision Date1985-12-10
Product CodeGEC
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

PHARMASEAL SCRUB CARE-SURGICAL SCRUB BRUSH SPONGES is the device name listed in this FDA 510(k) record. The listed applicant is American Pharmaseal Div. Ahsc. It received FDA 510(k) clearance on 1985-12-10 under 510(k) number K854232. The device is classified under product code GEC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the PHARMASEAL SCRUB CARE-SURGICAL SCRUB BRUSH SPONGES?

PHARMASEAL SCRUB CARE-SURGICAL SCRUB BRUSH SPONGES is a medical device that received FDA 510(k) clearance on 1985-12-10. The listed applicant is American Pharmaseal Div. Ahsc. The 510(k) number is K854232.

When did PHARMASEAL SCRUB CARE-SURGICAL SCRUB BRUSH SPONGES receive FDA 510(k) clearance?

PHARMASEAL SCRUB CARE-SURGICAL SCRUB BRUSH SPONGES received FDA 510(k) clearance on 1985-12-10, under 510(k) number K854232.

Who is the listed applicant for PHARMASEAL SCRUB CARE-SURGICAL SCRUB BRUSH SPONGES?

The FDA 510(k) record lists American Pharmaseal Div. Ahsc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHARMASEAL SCRUB CARE-SURGICAL SCRUB BRUSH SPONGES?

The FDA product code for PHARMASEAL SCRUB CARE-SURGICAL SCRUB BRUSH SPONGES is GEC.

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Other records listing American Pharmaseal Div. Ahsc as applicant

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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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