FDA 510(k)

SUPPLEMENTAL TYGON PAC-MONITORING LINES

K-Number: K780662 · 1978-06-06

ApplicantNorton Performance Plastics Corp.

Decision Date1978-06-06

Product CodeFMG

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SUPPLEMENTAL TYGON PAC-MONITORING LINES is the device name listed in this FDA 510(k) record. The listed applicant is Norton Performance Plastics Corp.. It received FDA 510(k) clearance on 1978-06-06 under 510(k) number K780662. The device is classified under product code FMG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPPLEMENTAL TYGON PAC-MONITORING LINES?

SUPPLEMENTAL TYGON PAC-MONITORING LINES is a medical device that received FDA 510(k) clearance on 1978-06-06. The listed applicant is Norton Performance Plastics Corp.. The 510(k) number is K780662.

When did SUPPLEMENTAL TYGON PAC-MONITORING LINES receive FDA 510(k) clearance?

SUPPLEMENTAL TYGON PAC-MONITORING LINES received FDA 510(k) clearance on 1978-06-06, under 510(k) number K780662.

Who is the listed applicant for SUPPLEMENTAL TYGON PAC-MONITORING LINES?

The FDA 510(k) record lists Norton Performance Plastics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUPPLEMENTAL TYGON PAC-MONITORING LINES?

The FDA product code for SUPPLEMENTAL TYGON PAC-MONITORING LINES is FMG.

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Other records listing Norton Performance Plastics Corp. as applicant

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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.