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FDA 510(k)

HARVARD/LTE LABORATORY STEAM STERILIZER AUTOCLAVE

K-Number: K903614 · 1990-12-14

Decision Date1990-12-14
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HARVARD/LTE LABORATORY STEAM STERILIZER AUTOCLAVE is the device name listed in this FDA 510(k) record. The listed applicant is Harvard Apparatus, Inc.. It received FDA 510(k) clearance on 1990-12-14 under 510(k) number K903614. The device is classified under product code FLE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HARVARD/LTE LABORATORY STEAM STERILIZER AUTOCLAVE?

HARVARD/LTE LABORATORY STEAM STERILIZER AUTOCLAVE is a medical device that received FDA 510(k) clearance on 1990-12-14. The listed applicant is Harvard Apparatus, Inc.. The 510(k) number is K903614.

When did HARVARD/LTE LABORATORY STEAM STERILIZER AUTOCLAVE receive FDA 510(k) clearance?

HARVARD/LTE LABORATORY STEAM STERILIZER AUTOCLAVE received FDA 510(k) clearance on 1990-12-14, under 510(k) number K903614.

Who is the listed applicant for HARVARD/LTE LABORATORY STEAM STERILIZER AUTOCLAVE?

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

What is the FDA product code for HARVARD/LTE LABORATORY STEAM STERILIZER AUTOCLAVE?

The FDA product code for HARVARD/LTE LABORATORY STEAM STERILIZER AUTOCLAVE is FLE.

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.

Other records listing Harvard Apparatus, 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.

View all 9 devices →

Related Devices (Code: FLE)

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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