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FDA 510(k)

ACCU-RYNGE PUMP SP-250

K-Number: K830389 · 1983-09-12

Decision Date1983-09-12
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ACCU-RYNGE PUMP SP-250 is the device name listed in this FDA 510(k) record. The listed applicant is Delta Medical Industries. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K830389. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCU-RYNGE PUMP SP-250?

ACCU-RYNGE PUMP SP-250 is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Delta Medical Industries. The 510(k) number is K830389.

When did ACCU-RYNGE PUMP SP-250 receive FDA 510(k) clearance?

ACCU-RYNGE PUMP SP-250 received FDA 510(k) clearance on 1983-09-12, under 510(k) number K830389.

Who is the listed applicant for ACCU-RYNGE PUMP SP-250?

The FDA 510(k) record lists Delta Medical Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACCU-RYNGE PUMP SP-250?

The FDA product code for ACCU-RYNGE PUMP SP-250 is FRN.

Related Clinical Trials

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.

Other records listing Delta Medical Industries 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.

View all 27 devices →

Related Devices (Code: FRN)

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.

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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