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FDA 510(k)

RENNCO MODEL LS LIFT SEAL HEAT SEALER

K-Number: K830540 · 1983-03-17

ApplicantRennco, Inc.
Decision Date1983-03-17
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RENNCO MODEL LS LIFT SEAL HEAT SEALER is the device name listed in this FDA 510(k) record. The listed applicant is Rennco, Inc.. It received FDA 510(k) clearance on 1983-03-17 under 510(k) number K830540. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RENNCO MODEL LS LIFT SEAL HEAT SEALER?

RENNCO MODEL LS LIFT SEAL HEAT SEALER is a medical device that received FDA 510(k) clearance on 1983-03-17. The listed applicant is Rennco, Inc.. The 510(k) number is K830540.

When did RENNCO MODEL LS LIFT SEAL HEAT SEALER receive FDA 510(k) clearance?

RENNCO MODEL LS LIFT SEAL HEAT SEALER received FDA 510(k) clearance on 1983-03-17, under 510(k) number K830540.

Who is the listed applicant for RENNCO MODEL LS LIFT SEAL HEAT SEALER?

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

What is the FDA product code for RENNCO MODEL LS LIFT SEAL HEAT SEALER?

The FDA product code for RENNCO MODEL LS LIFT SEAL HEAT SEALER is FRG.

Related Clinical Trials

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.

Related Devices (Code: FRG)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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