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FDA 510(k)

ULTRAPAK CAT. #100-0251

K-Number: K802690 · 1981-01-08

ApplicantOccumedics, Inc.
Decision Date1981-01-08
Product CodeHYG
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

ULTRAPAK CAT. #100-0251 is the device name listed in this FDA 510(k) record. The listed applicant is Occumedics, Inc.. It received FDA 510(k) clearance on 1981-01-08 under 510(k) number K802690. The device is classified under product code HYG. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRAPAK CAT. #100-0251?

ULTRAPAK CAT. #100-0251 is a medical device that received FDA 510(k) clearance on 1981-01-08. The listed applicant is Occumedics, Inc.. The 510(k) number is K802690.

When did ULTRAPAK CAT. #100-0251 receive FDA 510(k) clearance?

ULTRAPAK CAT. #100-0251 received FDA 510(k) clearance on 1981-01-08, under 510(k) number K802690.

Who is the listed applicant for ULTRAPAK CAT. #100-0251?

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

What is the FDA product code for ULTRAPAK CAT. #100-0251?

The FDA product code for ULTRAPAK CAT. #100-0251 is HYG.

Related Clinical Trials

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Other records listing Occumedics, 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.

K802691OCCUPAK CAT.#200-0538

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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