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FDA 510(k)

WESCOR STAIN PACK FOR MODEL 7100 AEROSPRAY SLIDE S

K-Number: K852138 · 1985-06-13

Decision Date1985-06-13
Product CodeIAF
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

WESCOR STAIN PACK FOR MODEL 7100 AEROSPRAY SLIDE S is the device name listed in this FDA 510(k) record. The listed applicant is Canyon Diagnostics, Inc.. It received FDA 510(k) clearance on 1985-06-13 under 510(k) number K852138. 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 WESCOR STAIN PACK FOR MODEL 7100 AEROSPRAY SLIDE S?

WESCOR STAIN PACK FOR MODEL 7100 AEROSPRAY SLIDE S is a medical device that received FDA 510(k) clearance on 1985-06-13. The listed applicant is Canyon Diagnostics, Inc.. The 510(k) number is K852138.

When did WESCOR STAIN PACK FOR MODEL 7100 AEROSPRAY SLIDE S receive FDA 510(k) clearance?

WESCOR STAIN PACK FOR MODEL 7100 AEROSPRAY SLIDE S received FDA 510(k) clearance on 1985-06-13, under 510(k) number K852138.

Who is the listed applicant for WESCOR STAIN PACK FOR MODEL 7100 AEROSPRAY SLIDE S?

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

What is the FDA product code for WESCOR STAIN PACK FOR MODEL 7100 AEROSPRAY SLIDE S?

The FDA product code for WESCOR STAIN PACK FOR MODEL 7100 AEROSPRAY SLIDE S 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 Canyon Diagnostics, 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: 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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