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FDA 510(k)

TASSAWAY

K-Number: K803250 · 1981-02-12

ApplicantPlastic Applications, Inc.
Decision Date1981-02-12
Product CodeHHE
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TASSAWAY is the device name listed in this FDA 510(k) record. The listed applicant is Plastic Applications, Inc.. It received FDA 510(k) clearance on 1981-02-12 under 510(k) number K803250. The device is classified under product code HHE. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TASSAWAY?

TASSAWAY is a medical device that received FDA 510(k) clearance on 1981-02-12. The listed applicant is Plastic Applications, Inc.. The 510(k) number is K803250.

When did TASSAWAY receive FDA 510(k) clearance?

TASSAWAY received FDA 510(k) clearance on 1981-02-12, under 510(k) number K803250.

Who is the listed applicant for TASSAWAY?

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

What is the FDA product code for TASSAWAY?

The FDA product code for TASSAWAY is HHE.

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Related Devices (Code: HHE)

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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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