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FDA 510(k)

TISSUE PROCESSING CASSETTES & ACCESS

K-Number: K813430 · 1981-12-29

ApplicantAmerican Optical Corp.
Decision Date1981-12-29
Product CodeIDL
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

TISSUE PROCESSING CASSETTES & ACCESS is the device name listed in this FDA 510(k) record. The listed applicant is American Optical Corp.. It received FDA 510(k) clearance on 1981-12-29 under 510(k) number K813430. The device is classified under product code IDL. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TISSUE PROCESSING CASSETTES & ACCESS?

TISSUE PROCESSING CASSETTES & ACCESS is a medical device that received FDA 510(k) clearance on 1981-12-29. The listed applicant is American Optical Corp.. The 510(k) number is K813430.

When did TISSUE PROCESSING CASSETTES & ACCESS receive FDA 510(k) clearance?

TISSUE PROCESSING CASSETTES & ACCESS received FDA 510(k) clearance on 1981-12-29, under 510(k) number K813430.

Who is the listed applicant for TISSUE PROCESSING CASSETTES & ACCESS?

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

What is the FDA product code for TISSUE PROCESSING CASSETTES & ACCESS?

The FDA product code for TISSUE PROCESSING CASSETTES & ACCESS is IDL.

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Other records listing American Optical Corp. 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.

K950881PHACO TIPK950880AOI UNIVERSAL ULTRASONIC HANDPIECEK931354P4000 PHACOEMULSIFIERK931358AORP4000 REUSABLE PAKK931357AOD4000 DISPOSABLE PAKK820790FLEXIBLE PROCTOSIGMOIDOSCOPE, #FPS-3

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Related Devices (Code: IDL)

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.

K863616KNIFE MAKERSurgipath Medical Industries, Inc.K831921DISPOSABLE MICROTOME BLADESPolymer Technology Corp.K831308DISPOSABLE MICROTOME BLADESurgipath Medical Industries, Inc.K801426TISSUE-TEK III MICROJECT DISP. BLADE SYSMiles Laboratories, Inc.

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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