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FDA 510(k)

SNOWDEN-PENCER IRRIGATION PUMP

K-Number: K920985 · 1992-06-09

ApplicantSnowden-Pencer
Decision Date1992-06-09
Product CodeHEI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SNOWDEN-PENCER IRRIGATION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Snowden-Pencer. It received FDA 510(k) clearance on 1992-06-09 under 510(k) number K920985. The device is classified under product code HEI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNOWDEN-PENCER IRRIGATION PUMP?

SNOWDEN-PENCER IRRIGATION PUMP is a medical device that received FDA 510(k) clearance on 1992-06-09. The listed applicant is Snowden-Pencer. The 510(k) number is K920985.

When did SNOWDEN-PENCER IRRIGATION PUMP receive FDA 510(k) clearance?

SNOWDEN-PENCER IRRIGATION PUMP received FDA 510(k) clearance on 1992-06-09, under 510(k) number K920985.

Who is the listed applicant for SNOWDEN-PENCER IRRIGATION PUMP?

The FDA 510(k) record lists Snowden-Pencer as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SNOWDEN-PENCER IRRIGATION PUMP?

The FDA product code for SNOWDEN-PENCER IRRIGATION PUMP is HEI.

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Other records listing Snowden-Pencer 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.

K960400DIAMOND-TOUCH AND MICRO DIAMOND-TOUCH INSTRUMENTS/DIAMOND-LINE INSTRUMENTS/DIAMOND-PORT(ACCESS PARTS)K930666REUSABLE LAPAROSCOPIC INSTRUMENTS W/ ELECTROCAUTERYK930667REUSABLE LAPAROSCOPIC INSTRUMENTSK924148DIAMOND-SHARP(R) TROCARSK924149ENDO I/A PROBEK920986SNOWDEN-PENCER HIGH FLOW INSUFFLATOR, SP/88-9700

View all 10 devices →

Related Devices (Code: HEI)

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.

K012003DRG REACTION CHAMBER/SAFETY TIPDoctor'S Research Group, Inc.K910982INNERVISION IRRIGATION PUMPM.D. Engineering, 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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