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FDA 510(k)

HISTO-TEK W/ AUTOMATIC COVERSLIPPER

K-Number: K761062 · 1977-03-07

ApplicantMiles Laboratories, Inc.
Decision Date1977-03-07
Product CodeIEO
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

HISTO-TEK W/ AUTOMATIC COVERSLIPPER is the device name listed in this FDA 510(k) record. The listed applicant is Miles Laboratories, Inc.. It received FDA 510(k) clearance on 1977-03-07 under 510(k) number K761062. The device is classified under product code IEO. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HISTO-TEK W/ AUTOMATIC COVERSLIPPER?

HISTO-TEK W/ AUTOMATIC COVERSLIPPER is a medical device that received FDA 510(k) clearance on 1977-03-07. The listed applicant is Miles Laboratories, Inc.. The 510(k) number is K761062.

When did HISTO-TEK W/ AUTOMATIC COVERSLIPPER receive FDA 510(k) clearance?

HISTO-TEK W/ AUTOMATIC COVERSLIPPER received FDA 510(k) clearance on 1977-03-07, under 510(k) number K761062.

Who is the listed applicant for HISTO-TEK W/ AUTOMATIC COVERSLIPPER?

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

What is the FDA product code for HISTO-TEK W/ AUTOMATIC COVERSLIPPER?

The FDA product code for HISTO-TEK W/ AUTOMATIC COVERSLIPPER is IEO.

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Related Devices (Code: IEO)

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.

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Official Source

View on FDA Database →

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

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