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FDA 510(k)

DRY SILVER PROCESSOR MODEL 1226

K-Number: K780640 · 1978-04-28

ApplicantHoneywell, Inc.
Decision Date1978-04-28
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DRY SILVER PROCESSOR MODEL 1226 is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1978-04-28 under 510(k) number K780640. The device is classified under product code DSF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRY SILVER PROCESSOR MODEL 1226?

DRY SILVER PROCESSOR MODEL 1226 is a medical device that received FDA 510(k) clearance on 1978-04-28. The listed applicant is Honeywell, Inc.. The 510(k) number is K780640.

When did DRY SILVER PROCESSOR MODEL 1226 receive FDA 510(k) clearance?

DRY SILVER PROCESSOR MODEL 1226 received FDA 510(k) clearance on 1978-04-28, under 510(k) number K780640.

Who is the listed applicant for DRY SILVER PROCESSOR MODEL 1226?

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

What is the FDA product code for DRY SILVER PROCESSOR MODEL 1226?

The FDA product code for DRY SILVER PROCESSOR MODEL 1226 is DSF.

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Other records listing Honeywell, 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.

K902230COLORADO COLOR IMAGING RECORDERK863100CEN STA MON AC/DC ALARM CENTRAL ACCES ALARM RECORK853501HONEYWELL ELECTRONIC VENTILATOR EV-AK855125PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEMK851888APM DISPOS. BLOOD PRESSURE TRANSDUCERK851496ECG MONITOR MODEL RM102

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Related Devices (Code: DSF)

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.

K910871EDENTEC DIGITAL CHARTER MODEL 3710Edentec Corp.K912929DASH IVAstro-Med, Inc.K905856MODEL 556 MONITORGe Medical Systems Information TechnologiesK902586GRI LASERGRAPH(TM) ECG PAPERGri Medical Products, Inc.K902230COLORADO COLOR IMAGING RECORDERHoneywell, Inc.K901385GABRIEL MEDICAL CLS THERMAL RECORDERGabriel Medical, 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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