FDA 510(k)

IMPULSE HEAT SEALER

K-Number: K760121 · 1976-07-16

Decision Date1976-07-16

Product Code

DecisionSubstantially Equivalent

Device Summary

IMPULSE HEAT SEALER is the device name listed in this FDA 510(k) record. The listed applicant is Lorvic Corp.. It received FDA 510(k) clearance on 1976-07-16 under 510(k) number K760121. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPULSE HEAT SEALER?

IMPULSE HEAT SEALER is a medical device that received FDA 510(k) clearance on 1976-07-16. The listed applicant is Lorvic Corp.. The 510(k) number is K760121.

When did IMPULSE HEAT SEALER receive FDA 510(k) clearance?

IMPULSE HEAT SEALER received FDA 510(k) clearance on 1976-07-16, under 510(k) number K760121.

Who is the listed applicant for IMPULSE HEAT SEALER?

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

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Other records listing Lorvic Corp. as applicant

K871615U. V. GERMICIDAL UNIT K780263SHIELD K770063DISP. ABSORBENT COMPRESSED FIBRE WAFER K770064FLUORIDE GEL DISPOSABLE TRAY K760620SALIVA EJECTOR

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.