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FDA 510(k)

WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMER

K-Number: K875275 · 1988-01-27

ApplicantSterling Drug, Inc.
Decision Date1988-01-27
Product CodeJTQ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMER is the device name listed in this FDA 510(k) record. The listed applicant is Sterling Drug, Inc.. It received FDA 510(k) clearance on 1988-01-27 under 510(k) number K875275. The device is classified under product code JTQ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMER?

WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMER is a medical device that received FDA 510(k) clearance on 1988-01-27. The listed applicant is Sterling Drug, Inc.. The 510(k) number is K875275.

When did WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMER receive FDA 510(k) clearance?

WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMER received FDA 510(k) clearance on 1988-01-27, under 510(k) number K875275.

Who is the listed applicant for WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMER?

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

What is the FDA product code for WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMER?

The FDA product code for WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMER is JTQ.

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Other records listing Sterling Drug, 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.

K901369GREEN LABEL BIOBRANE II AND RED LABEL BIOBRANE IIK896110BIOBRANE(R) IIK840260PERIOGRAF DURAPATITE 40-60 MESHK820023CONAGRAF TM DURAPATITE CONESK820164EMPTY STERILE CARPUJECTK813257ALVEOGRAF DURAPATITE(18-40 MESH)

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Related Devices (Code: JTQ)

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.

K853379PLATE INCUBATORScientific Sales Intl., Inc.K831592ANHYDRIC INCUBATORS, CULTURE INCUBATORBoekel Industries, Inc.K830322C.A.T. REAGENT KITRemel Co.K830227AUTOMATED ELISA READER LBI 300Bionetic Laboratory ProductsK830405LBI-100 37DEGREES INCUBATORBionetic Laboratory ProductsK822564WATER BATHBoekel Industries, 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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