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FDA 510(k)

STAIN PACK FOR AEROSPRAY SLIDE STAINER

K-Number: K833260 · 1983-10-28

ApplicantWescor, Inc.
Decision Date1983-10-28
Product CodeIAF
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

STAIN PACK FOR AEROSPRAY SLIDE STAINER is the device name listed in this FDA 510(k) record. The listed applicant is Wescor, Inc.. It received FDA 510(k) clearance on 1983-10-28 under 510(k) number K833260. The device is classified under product code IAF. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAIN PACK FOR AEROSPRAY SLIDE STAINER?

STAIN PACK FOR AEROSPRAY SLIDE STAINER is a medical device that received FDA 510(k) clearance on 1983-10-28. The listed applicant is Wescor, Inc.. The 510(k) number is K833260.

When did STAIN PACK FOR AEROSPRAY SLIDE STAINER receive FDA 510(k) clearance?

STAIN PACK FOR AEROSPRAY SLIDE STAINER received FDA 510(k) clearance on 1983-10-28, under 510(k) number K833260.

Who is the listed applicant for STAIN PACK FOR AEROSPRAY SLIDE STAINER?

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

What is the FDA product code for STAIN PACK FOR AEROSPRAY SLIDE STAINER?

The FDA product code for STAIN PACK FOR AEROSPRAY SLIDE STAINER is IAF.

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 Wescor, 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 13 devices →

Related Devices (Code: IAF)

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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