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FDA 510(k)

ACCUPAC CUSTOM SKIN SCRUB KIT

K-Number: K861219 · 1986-04-15

ApplicantGeneva Laboratories, Inc.
Decision Date1986-04-15
Product Code
DecisionSubstantially Equivalent

Device Summary

ACCUPAC CUSTOM SKIN SCRUB KIT is the device name listed in this FDA 510(k) record. The listed applicant is Geneva Laboratories, Inc.. It received FDA 510(k) clearance on 1986-04-15 under 510(k) number K861219. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCUPAC CUSTOM SKIN SCRUB KIT?

ACCUPAC CUSTOM SKIN SCRUB KIT is a medical device that received FDA 510(k) clearance on 1986-04-15. The listed applicant is Geneva Laboratories, Inc.. The 510(k) number is K861219.

When did ACCUPAC CUSTOM SKIN SCRUB KIT receive FDA 510(k) clearance?

ACCUPAC CUSTOM SKIN SCRUB KIT received FDA 510(k) clearance on 1986-04-15, under 510(k) number K861219.

Who is the listed applicant for ACCUPAC CUSTOM SKIN SCRUB KIT?

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

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Other records listing Geneva Laboratories, 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.

K881217GENT-L-KARE STERILE URINARY LEG BAGK881213GENT-L-KARE STERILE URINARY DRAINAGE BAG CENTERK881218GENT-L-KARE CLEANSING ENEMA SETK881216GENT-L-KARE VAGINAL IRRIGATION SETK861308ACCUPAC CUSTOM PACK KERLIX SQUARESK853265ACCUPAC CUSTOM OPERATING ROOM PROCEDURE-DK876543

View all 13 devices →

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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