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FDA 510(k)

TISSUE-TEK V.I.P. 100/200

K-Number: K831313 · 1983-07-28

ApplicantMiles Laboratories, Inc.
Decision Date1983-07-28
Product CodeIEO
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

TISSUE-TEK V.I.P. 100/200 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 1983-07-28 under 510(k) number K831313. 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 TISSUE-TEK V.I.P. 100/200?

TISSUE-TEK V.I.P. 100/200 is a medical device that received FDA 510(k) clearance on 1983-07-28. The listed applicant is Miles Laboratories, Inc.. The 510(k) number is K831313.

When did TISSUE-TEK V.I.P. 100/200 receive FDA 510(k) clearance?

TISSUE-TEK V.I.P. 100/200 received FDA 510(k) clearance on 1983-07-28, under 510(k) number K831313.

Who is the listed applicant for TISSUE-TEK V.I.P. 100/200?

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 TISSUE-TEK V.I.P. 100/200?

The FDA product code for TISSUE-TEK V.I.P. 100/200 is IEO.

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Other records listing Miles Laboratories, Inc. as applicant

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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.

K924590MICROWAVE AUTOMATED TISSUE PROCESSORInnovative Medical Systems, Inc.K883599LX-80 AUTOMATED TISSUE PROCESSOR (PLASTIC)Innovative Medical Systems, Inc.K881165SAKURA HEM-480 ELECTRON MICROSCOPY PROCESSORSakura Finetek U.S.A., Inc.K853938LX 300 TISSUE PROCESSORInnovative Medical Systems, Inc.K851054LX120 TISSUE PROCESSORInnovative Medical Systems, Inc.K843506LKB 2189 ULTROPROCESSORLkb Instruments, 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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